Align Acetylornithine/succinyldiaminopimelate aminotransferase; ACOAT; DapATase; Succinyldiaminopimelate transferase; EC 2.6.1.11; EC 2.6.1.17 (characterized)
to candidate H281DRAFT_06478 H281DRAFT_06478 succinylornithine aminotransferase apoenzyme
Query= SwissProt::P18335 (406 letters) >lcl|FitnessBrowser__Burk376:H281DRAFT_06478 H281DRAFT_06478 succinylornithine aminotransferase apoenzyme Length = 411 Score = 490 bits (1262), Expect = e-143 Identities = 232/398 (58%), Positives = 299/398 (75%) Query: 8 ITRATFDEVILPIYAPAEFIPVKGQGSRIWDQQGKEYVDFAGGIAVTALGHCHPALVNAL 67 +TR TFDEV++P++APA F+P +G GSR+WD QG++Y+DFAGGIAVTALGH HP L+ L Sbjct: 6 VTRKTFDEVMVPVFAPAAFVPDRGLGSRVWDTQGRDYIDFAGGIAVTALGHAHPELLKVL 65 Query: 68 KTQGETLWHISNVFTNEPALRLGRKLIEATFAERVVFMNSGTEANETAFKLARHYACVRH 127 QG LWHI N +TNEP LRL R+L E TFA+R F NSG EANE A KLAR A RH Sbjct: 66 HEQGSKLWHIGNGYTNEPVLRLARRLEELTFADRAFFANSGAEANEAALKLARRVAFERH 125 Query: 128 SPFKTKIIAFHNAFHGRSLFTVSVGGQPKYSDGFGPKPADIIHVPFNDLHAVKAVMDDHT 187 K +II+F +FHGR+ FTVSVGGQPKYS+GFGP P I+H+P+ND+ A + + T Sbjct: 126 GADKYEIISFTQSFHGRTFFTVSVGGQPKYSEGFGPVPQGIVHLPYNDIQAAQKAIGAKT 185 Query: 188 CAVVVEPIQGEGGVTAATPEFLQGLRELCDQHQALLVFDEVQCGMGRTGDLFAYMHYGVT 247 CAV+VEPIQGEGGV A P FL+ LRE CDQH ALL+FDEVQ G+GR+G +AY GVT Sbjct: 186 CAVIVEPIQGEGGVIPADPAFLKALREACDQHGALLIFDEVQTGVGRSGYFYAYQDTGVT 245 Query: 248 PDILTSAKALGGGFPISAMLTTAEIASAFHPGSHGSTYGGNPLACAVAGAAFDIINTPEV 307 PDILT+AKALG GFPI AMLTT E+A+ F G HG+TYGGNPL A+A ++I+ P++ Sbjct: 246 PDILTTAKALGNGFPIGAMLTTNELAAHFKVGVHGTTYGGNPLGSAIAEKVVELISDPKL 305 Query: 308 LEGIQAKRQRFVDHLQKIDQQYDVFSDIRGMGLLIGAELKPQYKGRARDFLYAGAEAGVM 367 LEG++ + + HL K+++++ +F ++RG GLLIGA+L YKGRA+DF+ A + GV+ Sbjct: 306 LEGVRTRSEVLKGHLAKLNERFGLFDEVRGKGLLIGAQLTDAYKGRAKDFVTAAGQHGVI 365 Query: 368 VLNAGPDVMRFAPSLVVEDADIDEGMQRFAHAVAKVVG 405 +L AGPDV+RF PSL++ D++EG +R A A+A VVG Sbjct: 366 MLMAGPDVLRFVPSLIMPLDDMNEGFERLAKAIADVVG 403 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: 561 Number of extensions: 19 Number of successful extensions: 1 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: 411 Length adjustment: 31 Effective length of query: 375 Effective length of database: 380 Effective search space: 142500 Effective search space used: 142500 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