Align N-succinyldiaminopimelate-aminotransferase (EC 2.6.1.17) (characterized)
to candidate PfGW456L13_4713 N-succinyl-L,L-diaminopimelate aminotransferase alternative (EC 2.6.1.17)
Query= metacyc::MONOMER-6501 (397 letters) >FitnessBrowser__pseudo13_GW456_L13:PfGW456L13_4713 Length = 399 Score = 413 bits (1062), Expect = e-120 Identities = 217/395 (54%), Positives = 264/395 (66%), Gaps = 4/395 (1%) Query: 1 MNPRLDALHPYPFEKLRALLADAGKPTHDLPPINLSIGEPKHAAPACVGQAIAANLAGLS 60 MN L L PYPFEKLRALL P D PI LSIGEPKH +P+ V +A+A NL ++ Sbjct: 1 MNNALSQLQPYPFEKLRALLGSV-TPNPDKRPIALSIGEPKHRSPSFVAEALAGNLEKMA 59 Query: 61 VYPSTKGEPALRQAISQWLSRRYSIPAP--DPESEVLPVLGSREALFAFAQTVIDPSAGA 118 VYP+T G P LR+AI+ W RR+ +P DP VLPV G+REALFAF QTV++ A Sbjct: 60 VYPTTLGIPELREAIAAWCERRFDVPKGWIDPARNVLPVNGTREALFAFTQTVVNRGDDA 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 + FVIAA ECYSE+Y DE TPP G L A LGR + V Sbjct: 180 TGALIPVETLKKLIALADEYDFVIAADECYSELYFDEQTPPPGLLSACAELGRKDFKRCV 239 Query: 239 AFSSLSKRSNVPGMRSGFVAGDAALLARFLLYRTYHGSAMSPVVSAASIAAWSMRRMCR- 297 F SLSKRSN+PG+RSGFVAGDA +L FLLYRTYHG AM AS+AAW+ R Sbjct: 240 VFHSLSKRSNLPGLRSGFVAGDADVLKGFLLYRTYHGCAMPVQTQLASVAAWNDEVHVRA 299 Query: 298 KTAQYRAKFEAVLPILQNVLDVRAPQASFYLWAGTPGSDTAFARELYGRTGVTVLPGSLL 357 A YR KF+AVL IL VLDV+ P SFYLW G D AF R+L+ + VTV+PGS L Sbjct: 300 NRALYREKFDAVLEILSPVLDVQRPDGSFYLWPNVAGDDAAFCRDLFEQEHVTVVPGSYL 359 Query: 358 AREAHNANPGQGRIRIALVAPLDQCVQAAERIAHF 392 +R+ NPG GR+R+ALVAPL +CV+AAERI F Sbjct: 360 SRDVDGVNPGAGRVRMALVAPLAECVEAAERIRDF 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: 512 Number of extensions: 27 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 PfGW456L13_4713 (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.7868.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 ------- ------ ----- ------- ------ ----- ---- -- -------- ----------- 1.3e-212 691.7 0.0 1.5e-212 691.6 0.0 1.0 1 lcl|FitnessBrowser__pseudo13_GW456_L13:PfGW456L13_4713 N-succinyl-L,L-diaminopimelate a Domain annotation for each sequence (and alignments): >> lcl|FitnessBrowser__pseudo13_GW456_L13:PfGW456L13_4713 N-succinyl-L,L-diaminopimelate aminotransferase alternative ( # score bias c-Evalue i-Evalue hmmfrom hmm to alifrom ali to envfrom env to acc --- ------ ----- --------- --------- ------- ------- ------- ------- ------- ------- ---- 1 ! 691.6 0.0 1.5e-212 1.5e-212 1 395 [] 1 395 [. 1 395 [. 1.00 Alignments for each domain: == domain 1 score: 691.6 bits; conditional E-value: 1.5e-212 TIGR03538 1 mnpnlerlkpyPfeklaellkdvtppadleeialsiGePkhatPafvlealvenl 55 mn++l++l+pyPfekl++ll +vtp+ d+++ialsiGePkh++P+fv+eal+ nl lcl|FitnessBrowser__pseudo13_GW456_L13:PfGW456L13_4713 1 MNNALSQLQPYPFEKLRALLGSVTPNPDKRPIALSIGEPKHRSPSFVAEALAGNL 55 9****************************************************** PP TIGR03538 56 eelskyPttkGlpelreaiaeWlerrfelpag.vdperqvlPvnGtrealfafvq 109 e+++ yPtt G+pelreaia+W+errf++p+g +dp+r+vlPvnGtrealfaf+q lcl|FitnessBrowser__pseudo13_GW456_L13:PfGW456L13_4713 56 EKMAVYPTTLGIPELREAIAAWCERRFDVPKGwIDPARNVLPVNGTREALFAFTQ 110 ******************************************************* PP TIGR03538 110 avidraekalvvlPnPfyqiyeGaallagaepyflnctaengfkpdfdavpeevW 164 +v++r ++alvv+PnPfyqiyeGaa+laga+p++l+c +engf+pdfdav+ ++W lcl|FitnessBrowser__pseudo13_GW456_L13:PfGW456L13_4713 111 TVVNRGDDALVVSPNPFYQIYEGAAFLAGAKPHYLPCLDENGFNPDFDAVSPDIW 165 ******************************************************* PP TIGR03538 165 krvqllfvcsPgnPtGavlsleelkklleladkydfiiasdecyselyldeaeaP 219 kr+q+lf+csPgnPtGa++++e+lkkl++lad+ydf+ia+decysely+de+++P lcl|FitnessBrowser__pseudo13_GW456_L13:PfGW456L13_4713 166 KRCQILFLCSPGNPTGALIPVETLKKLIALADEYDFVIAADECYSELYFDEQTPP 220 ******************************************************* PP TIGR03538 220 vGlleaaaelGrddfkrllvfhslskrsnvPGlrsGfvaGdaellkeflryrtyh 274 Gll+a+aelGr+dfkr++vfhslskrsn+PGlrsGfvaGda++lk fl yrtyh lcl|FitnessBrowser__pseudo13_GW456_L13:PfGW456L13_4713 221 PGLLSACAELGRKDFKRCVVFHSLSKRSNLPGLRSGFVAGDADVLKGFLLYRTYH 275 ******************************************************* PP TIGR03538 275 GcampiavqlasiaaWedekhvrenralyrekfaavleilgavldlelPdasfyl 329 Gcamp+++qlas+aaW+de hvr+nralyrekf+avleil++vld+++Pd+sfyl lcl|FitnessBrowser__pseudo13_GW456_L13:PfGW456L13_4713 276 GCAMPVQTQLASVAAWNDEVHVRANRALYREKFDAVLEILSPVLDVQRPDGSFYL 330 ******************************************************* PP TIGR03538 330 WlkvpdgddeafaralyeeenvkvlpGrylsreaegvnPGegrvrlalvaeleec 384 W++v gdd+af+r+l+e+e+v+v+pG+ylsr+++gvnPG+grvr+alva+l+ec lcl|FitnessBrowser__pseudo13_GW456_L13:PfGW456L13_4713 331 WPNV-AGDDAAFCRDLFEQEHVTVVPGSYLSRDVDGVNPGAGRVRMALVAPLAEC 384 ****.7************************************************* PP TIGR03538 385 veaaerikkll 395 veaaeri++++ lcl|FitnessBrowser__pseudo13_GW456_L13:PfGW456L13_4713 385 VEAAERIRDFI 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: 0.01u 0.01s 00:00:00.02 Elapsed: 00:00:00.01 # Mc/sec: 12.14 // [ok]
This GapMind analysis is from Apr 09 2024. The underlying query database was built on Apr 09 2024.
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:
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