Align succinyldiaminopimelate transaminase (EC 2.6.1.17) (characterized)
to candidate Pf1N1B4_3080 N-succinyl-L,L-diaminopimelate aminotransferase alternative (EC 2.6.1.17)
Query= BRENDA::Q9ZEX3 (397 letters) >FitnessBrowser__pseudo1_N1B4:Pf1N1B4_3080 Length = 399 Score = 412 bits (1059), Expect = e-120 Identities = 217/395 (54%), Positives = 266/395 (67%), Gaps = 4/395 (1%) Query: 1 MNPRLDALHPYPFEKLRALLADAGKPTHDLPPINLSIGEPKHAAPACVGQAIAANLAGLS 60 MN L+ L PYPFEKLRALL P D I LSIGEPKH +PA V +A+A+NL ++ Sbjct: 1 MNNALNQLQPYPFEKLRALLGSV-TPNPDKRAIALSIGEPKHRSPAFVAEALASNLDQMA 59 Query: 61 VYPSTKGEPALRQAISQWLSRRYSIPAP--DPESEVLPVLGSREALFAFAQTVIDPSAGA 118 VYP+T G PALR+AI+ W RR+S+P DP VLPV G+REALFAF QTV++ A Sbjct: 60 VYPTTLGIPALREAIAAWCERRFSVPNGWLDPARNVLPVNGTREALFAFTQTVVNRGDDA 119 Query: 119 LVVCPNPFYQIYEGAALLAGATPYYVNADPARDFGLRTGRVPDEVWRRTQLVFVCSPGNP 178 LVV PNPFYQIYEGAA LAGA P+Y+ F V ++W+R Q++F+CSPGNP Sbjct: 120 LVVSPNPFYQIYEGAAFLAGAKPHYLPCLDENGFNPDFDAVSPDIWKRCQILFLCSPGNP 179 Query: 179 AGNVMSLEEWRTLFELSDRHGFVIAAYECYSEIYLDEDTPPLGSLQAARRLGRDRYTNLV 238 G ++ +E + L L+D H FVIAA ECYSE+Y DE TPP G L A LGR + V Sbjct: 180 TGALIPVETLKKLIALADEHDFVIAADECYSELYFDEQTPPAGLLSACVELGRKDFKRCV 239 Query: 239 AFSSLSKRSNVPGMRSGFVAGDAALLARFLLYRTYHGSAMSPVVSAASIAAWSMRRMCR- 297 F SLSKRSN+PG+RSGFVAGDA +L FLLYRTYHG AM AS+AAW+ R Sbjct: 240 VFHSLSKRSNLPGLRSGFVAGDADILKGFLLYRTYHGCAMPVQTQLASVAAWNDEVHVRA 299 Query: 298 KTAQYRAKFEAVLPILQNVLDVRAPQASFYLWAGTPGSDTAFARELYGRTGVTVLPGSLL 357 A YR K++AVL IL V++V+ P FYLW G D AF R+L+ + VTV+PGS L Sbjct: 300 NRALYREKYDAVLEILSPVMEVQRPDGGFYLWPNVNGDDAAFCRDLFEQEHVTVVPGSYL 359 Query: 358 AREAHNANPGQGRIRIALVAPLDQCVQAAERIAHF 392 +R+ NPG GRIR+ALVAPL +CV+AAERI F Sbjct: 360 SRDVDGVNPGAGRIRMALVAPLAECVEAAERIRAF 394 Lambda K H 0.321 0.135 0.412 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: 507 Number of extensions: 28 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: 397 Length of database: 399 Length adjustment: 31 Effective length of query: 366 Effective length of database: 368 Effective search space: 134688 Effective search space used: 134688 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)
Align candidate Pf1N1B4_3080 (N-succinyl-L,L-diaminopimelate aminotransferase alternative (EC 2.6.1.17))
to HMM TIGR03538 (dapC: succinyldiaminopimelate transaminase (EC 2.6.1.17))
# hmmsearch :: search profile(s) against a sequence database # HMMER 3.3.1 (Jul 2020); http://hmmer.org/ # Copyright (C) 2020 Howard Hughes Medical Institute. # Freely distributed under the BSD open source license. # - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - # query HMM file: ../tmp/path.aa/TIGR03538.hmm # target sequence database: /tmp/gapView.6896.genome.faa # - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - Query: TIGR03538 [M=395] Accession: TIGR03538 Description: DapC_gpp: succinyldiaminopimelate transaminase Scores for complete sequences (score includes all domains): --- full sequence --- --- best 1 domain --- -#dom- E-value score bias E-value score bias exp N Sequence Description ------- ------ ----- ------- ------ ----- ---- -- -------- ----------- 5.9e-211 686.3 0.0 6.6e-211 686.1 0.0 1.0 1 lcl|FitnessBrowser__pseudo1_N1B4:Pf1N1B4_3080 N-succinyl-L,L-diaminopimelate a Domain annotation for each sequence (and alignments): >> lcl|FitnessBrowser__pseudo1_N1B4:Pf1N1B4_3080 N-succinyl-L,L-diaminopimelate aminotransferase alternative (EC 2.6.1. # score bias c-Evalue i-Evalue hmmfrom hmm to alifrom ali to envfrom env to acc --- ------ ----- --------- --------- ------- ------- ------- ------- ------- ------- ---- 1 ! 686.1 0.0 6.6e-211 6.6e-211 1 395 [] 1 395 [. 1 395 [. 1.00 Alignments for each domain: == domain 1 score: 686.1 bits; conditional E-value: 6.6e-211 TIGR03538 1 mnpnlerlkpyPfeklaellkdvtppadleeialsiGePkhatPafvlealvenleelskyPtt 64 mn++l++l+pyPfekl++ll +vtp+ d+++ialsiGePkh++Pafv+eal++nl++++ yPtt lcl|FitnessBrowser__pseudo1_N1B4:Pf1N1B4_3080 1 MNNALNQLQPYPFEKLRALLGSVTPNPDKRAIALSIGEPKHRSPAFVAEALASNLDQMAVYPTT 64 9*************************************************************** PP TIGR03538 65 kGlpelreaiaeWlerrfelpag.vdperqvlPvnGtrealfafvqavidraekalvvlPnPfy 127 G+p+lreaia+W+errf++p+g +dp+r+vlPvnGtrealfaf+q+v++r ++alvv+PnPfy lcl|FitnessBrowser__pseudo1_N1B4:Pf1N1B4_3080 65 LGIPALREAIAAWCERRFSVPNGwLDPARNVLPVNGTREALFAFTQTVVNRGDDALVVSPNPFY 128 **************************************************************** PP TIGR03538 128 qiyeGaallagaepyflnctaengfkpdfdavpeevWkrvqllfvcsPgnPtGavlsleelkkl 191 qiyeGaa+laga+p++l+c +engf+pdfdav+ ++Wkr+q+lf+csPgnPtGa++++e+lkkl lcl|FitnessBrowser__pseudo1_N1B4:Pf1N1B4_3080 129 QIYEGAAFLAGAKPHYLPCLDENGFNPDFDAVSPDIWKRCQILFLCSPGNPTGALIPVETLKKL 192 **************************************************************** PP TIGR03538 192 leladkydfiiasdecyselyldeaeaPvGlleaaaelGrddfkrllvfhslskrsnvPGlrsG 255 ++lad++df+ia+decysely+de+++P+Gll+a+ elGr+dfkr++vfhslskrsn+PGlrsG lcl|FitnessBrowser__pseudo1_N1B4:Pf1N1B4_3080 193 IALADEHDFVIAADECYSELYFDEQTPPAGLLSACVELGRKDFKRCVVFHSLSKRSNLPGLRSG 256 **************************************************************** PP TIGR03538 256 fvaGdaellkeflryrtyhGcampiavqlasiaaWedekhvrenralyrekfaavleilgavld 319 fvaGda++lk fl yrtyhGcamp+++qlas+aaW+de hvr+nralyrek++avleil++v++ lcl|FitnessBrowser__pseudo1_N1B4:Pf1N1B4_3080 257 FVAGDADILKGFLLYRTYHGCAMPVQTQLASVAAWNDEVHVRANRALYREKYDAVLEILSPVME 320 **************************************************************** PP TIGR03538 320 lelPdasfylWlkvpdgddeafaralyeeenvkvlpGrylsreaegvnPGegrvrlalvaelee 383 +++Pd++fylW++v +gdd+af+r+l+e+e+v+v+pG+ylsr+++gvnPG+gr+r+alva+l+e lcl|FitnessBrowser__pseudo1_N1B4:Pf1N1B4_3080 321 VQRPDGGFYLWPNV-NGDDAAFCRDLFEQEHVTVVPGSYLSRDVDGVNPGAGRIRMALVAPLAE 383 **************.8************************************************ PP TIGR03538 384 cveaaerikkll 395 cveaaeri++++ lcl|FitnessBrowser__pseudo1_N1B4:Pf1N1B4_3080 384 CVEAAERIRAFI 395 *********996 PP Internal pipeline statistics summary: ------------------------------------- Query model(s): 1 (395 nodes) Target sequences: 1 (399 residues searched) Passed MSV filter: 1 (1); expected 0.0 (0.02) Passed bias filter: 1 (1); expected 0.0 (0.02) Passed Vit filter: 1 (1); expected 0.0 (0.001) Passed Fwd filter: 1 (1); expected 0.0 (1e-05) Initial search space (Z): 1 [actual number of targets] Domain search space (domZ): 1 [number of targets reported over threshold] # CPU time: 0.02u 0.01s 00:00:00.03 Elapsed: 00:00:00.02 # Mc/sec: 7.26 // [ok]
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