Align Acetylornithine/succinyldiaminopimelate aminotransferase; ACOAT; DapATase; Succinyldiaminopimelate transferase; EC 2.6.1.11; EC 2.6.1.17 (characterized)
to candidate 6938533 Sama_2636 4-aminobutyrate aminotransferase (RefSeq)
Query= SwissProt::P18335 (406 letters) >FitnessBrowser__SB2B:6938533 Length = 425 Score = 218 bits (556), Expect = 2e-61 Identities = 140/406 (34%), Positives = 207/406 (50%), Gaps = 41/406 (10%) Query: 30 KGQGSRIWDQQGKEYVDFAGGIAVTALGHCHPALVNALKTQGETLWHIS-NVFTNEPALR 88 + + + +WD +G+EY+DFAGGIAV GH HP + A+ Q E H V E + Sbjct: 30 RAENATVWDVEGREYIDFAGGIAVLNTGHLHPKVKAAVAEQLEKFSHTCFMVLGYESYVA 89 Query: 89 LGRKL---IEATFAERVVFMNSGTEANETAFKLARHYACVRHSPFKTKIIAFHNAFHGRS 145 + KL + FA++ SG+EA E A K+AR Y + +IAF + +HGR+ Sbjct: 90 VCEKLNQLVPGDFAKKSALFTSGSEAVENAIKVARAYTK------RAGVIAFTSGYHGRT 143 Query: 146 LFTVSVGGQ-PKYSDGFGPKPADIIHVPFN-DLHAVKAVMDD----------------HT 187 + +++ G+ YS G G A++ F LH V DD Sbjct: 144 MAALALTGKVAPYSKGMGLMQANVFRAEFPCALHGVSE--DDAMASIERIFKNDAEPSDI 201 Query: 188 CAVVVEPIQGEGGVTAATPEFLQGLRELCDQHQALLVFDEVQCGMGRTGDLFAYMHYGVT 247 A+++EP+QGEGG AATP F++ LRELCD+ +L+ DEVQ G GRTG FA GV Sbjct: 202 AAIILEPVQGEGGFYAATPGFMKRLRELCDREGIMLIADEVQTGAGRTGTFFAMEQMGVA 261 Query: 248 PDILTSAKALGGGFPISAMLTTAEIASAFHPGSHGSTYGGNPLACAVAGAAFDIINTPEV 307 DI T AK++ GGFP+S + AE+ A PG G TYGG+PLACA A A ++ ++ Sbjct: 262 ADITTFAKSIAGGFPLSGITGRAEVMDAIGPGGLGGTYGGSPLACAAALAVIEVFEEEKL 321 Query: 308 LEGIQAKRQRFVDHLQKIDQQYDVFSDIRGMGLLIGAEL------KPQYKGRARDFLYAG 361 LE A Q + ++ +Y +++RG+G +I EL P+Y L Sbjct: 322 LERSNAIGQTIKSAIGELASRYPQIAEVRGLGSMIAIELMENGKPAPEY---CPQVLTEA 378 Query: 362 AEAGVMVLNAGP--DVMRFAPSLVVEDADIDEGMQRFAHAVAKVVG 405 G+++L+ G +V+R + D I G++ A V+G Sbjct: 379 RNRGLILLSCGTYGNVLRILVPITAPDEQIQRGLEIMAECFEAVLG 424 Lambda K H 0.322 0.138 0.415 Gapped Lambda K H 0.267 0.0410 0.140 Matrix: BLOSUM62 Gap Penalties: Existence: 11, Extension: 1 Number of Sequences: 1 Number of Hits to DB: 458 Number of extensions: 21 Number of successful extensions: 4 Number of sequences better than 1.0e-02: 1 Number of HSP's gapped: 1 Number of HSP's successfully gapped: 1 Length of query: 406 Length of database: 425 Length adjustment: 31 Effective length of query: 375 Effective length of database: 394 Effective search space: 147750 Effective search space used: 147750 Neighboring words threshold: 11 Window for multiple hits: 40 X1: 16 ( 7.4 bits) X2: 38 (14.6 bits) X3: 64 (24.7 bits) S1: 41 (21.9 bits) S2: 50 (23.9 bits)
This GapMind analysis is from Aug 03 2021. The underlying query database was built on Aug 03 2021.
Each pathway is defined by a set of rules based on individual steps or genes. Candidates for each step are identified by using ublast (a fast alternative to protein BLAST) against a database of manually-curated proteins (most of which are experimentally characterized) or by using HMMer with enzyme models (usually from TIGRFam). Ublast hits may be split across two different proteins.
A candidate for a step is "high confidence" if either:
Otherwise, a candidate is "medium confidence" if either:
Other blast hits with at least 50% coverage are "low confidence."
Steps with no high- or medium-confidence candidates may be considered "gaps." For the typical bacterium that can make all 20 amino acids, there are 1-2 gaps in amino acid biosynthesis pathways. For diverse bacteria and archaea that can utilize a carbon source, there is a complete high-confidence catabolic pathway (including a transporter) just 38% of the time, and there is a complete medium-confidence pathway 63% of the time. Gaps may be due to:
GapMind relies on the predicted proteins in the genome and does not search the six-frame translation. In most cases, you can search the six-frame translation by clicking on links to Curated BLAST for each step definition (in the per-step page).
For more information, see the paper from 2019 on GapMind for amino acid biosynthesis, the paper from 2022 on GapMind for carbon sources, or view the source code, or see changes to Amino acid biosynthesis since the publication.
If you notice any errors or omissions in the step descriptions, or any questionable results, please let us know
by Morgan Price, Arkin group, Lawrence Berkeley National Laboratory