The pathway with the name 2-Aminobenzoate
 has the following structure: 
Result: 
CC(C)(COP(=O)(O)OP(=O)(O)OC[C@@H]1[C@H]([C@H]([C@H](N2C=NC3=C2N=CN=C3N)O1)O)OP(=O)(O)O)[C@H](C(=O)NCCC(=O)NCCSC(=O)C4=C(C=CC=C4)N)O
 no rule associatedCC(C)(COP(=O)(O)OP(=O)(O)OCC1C(C(C(N2C=NC3=C2N=CN=C3N)O1)O)OP(=O)(O)O)C(C(=O)NCCC(=O)NCCSC(=O)C4=C(CCC(=O)C4)N)O
C1=CC(=C(C=C1)N)C(=O)[O-]
 SimpleRule(uri = https://envipath.org/package/32de3cf4-e3e6-4168-956e-32fa5ddb0ce1/simple-rule/42add347-d29c-4ac9-9b35-89308c3b1bd6, SMIRKS = [H][c:2](:[c:7]):[c:1](:[c:6])-[#7;!$(NC(N)=O)!$(N(C=O)c1ccccc1C):5](-[#1,#6:9])-[#1,#6:10]>>[#8]-[c:1](:[c:6]):[c:2](-[#8]):[c:7].[#1,#6:10]-[#7:5]-[#1,#6:9]) C1=CC(=C(C(=C1)C(=O)[O-])O)O
CC(C)(COP(=O)(O)OP(=O)(O)OCC1C(C(C(N2C=NC3=C2N=CN=C3N)O1)O)OP(=O)(O)O)C(C(=O)NCCC(=O)NCCSC(=O)C4=C(CCC(=O)C4)N)O
 no rule associatedCC(C)(COP(=O)(O)OP(=O)(O)OC[C@@H]1[C@H]([C@H]([C@H](N2C=NC3=C2N=CN=C3N)O1)O)OP(=O)(O)O)[C@H](C(=O)NCCC(=O)NCCS)O
C1CC(=O)CCC1=O
C1=CC(=C(C=C1)N)C(=O)[O-]
 SimpleRule(uri = https://envipath.org/package/32de3cf4-e3e6-4168-956e-32fa5ddb0ce1/simple-rule/620525f2-3dfe-461f-b2b5-56e4fb4ffd88, SMIRKS = [#8-]-[#6](=O)-[c:1]1[c:12][c:11][c:10][c:9][c:8]1-[#7H2,#8H1]>>[#8]([H])-[c:8]1[c:9][c:10][c:11][c:12][c:1]1-[#8]([H])) C1=CC(=C(C=C1)O)O
C1=CC(=C(C=C1)N)C(=O)[O-]
 no rule associatedCC(C)(COP(=O)(O)OP(=O)(O)OC[C@@H]1[C@H]([C@H]([C@H](N2C=NC3=C2N=CN=C3N)O1)O)OP(=O)(O)O)[C@H](C(=O)NCCC(=O)NCCSC(=O)C4=C(C=CC=C4)N)O
C1=CC(=C(C(=C1)C(=O)[O-])O)O
 SimpleRule(uri = https://envipath.org/package/32de3cf4-e3e6-4168-956e-32fa5ddb0ce1/simple-rule/d6ccc928-0bff-478b-b674-5bb3bb8d319d, SMIRKS = [O-]-[C](=O)-[c;!$(c1(C(=O)[O-])ccccn1)!$(c1(C(=O)[O-])cccnc1):1](:[#6,#7,#8,#16;a:5]):[c:6]>>[#6,#7,#8,#16;a:5]:[c:1]:[c:6]) C1=CC(=C(C=C1)O)O

Description: 2-Aminobenzoate is an intermediate derived from tryptophan and other indole ring-containing compounds. The catabolism of 2-aminobenzoic acid has been well-studied. Here we only addressed the aerobic biodegradation pathway, the anaerobic pathway is documented elsewhere in the UMBBD. Pseudomonas sp. KB740 transforms 2-aminobenzoate to 1,4-cyclohexadione via 2-amino-5-oxo-cyclohex-1-enecarboxy-CoA ([http://www.ncbi.nlm.nih.gov/pubmed/1885526|Altenschmidt et al., 1991]). Other pseudomonads transform it directly to catechol ([http://www.ncbi.nlm.nih.gov/pubmed/14209949|Taniuchi et al., 1964]). The fungus Aspergillus niger takes two steps to get to the same end ([http://www.ncbi.nlm.nih.gov/pubmed/2310183|Kamath & Vaidyanathan, 1990]).
Your Options:
Update the Pathway Information: POST with (required) pathwayName and (optional) pathwayDescription.
Delete the Pathway: DELETE.
Show nodes: GET on https://envipath.org/package/32de3cf4-e3e6-4168-956e-32fa5ddb0ce1/pathway/dfc8c935-9d73-4067-bfe6-db3501d2075f/node
Show edges: GET on https://envipath.org/package/32de3cf4-e3e6-4168-956e-32fa5ddb0ce1/pathway/dfc8c935-9d73-4067-bfe6-db3501d2075f/edge