Align Gamma-glutamyl phosphate reductase; GPR; Glutamate-5-semialdehyde dehydrogenase; Glutamyl-gamma-semialdehyde dehydrogenase; GSA dehydrogenase; EC 1.2.1.41 (characterized)
to candidate 5210587 Shew_3015 gamma-glutamyl phosphate reductase (RefSeq)
Query= SwissProt::P07004 (417 letters) >FitnessBrowser__PV4:5210587 Length = 415 Score = 341 bits (875), Expect = 2e-98 Identities = 183/417 (43%), Positives = 259/417 (62%), Gaps = 4/417 (0%) Query: 1 MLEQMGIAAKQASYKLAQLSSREKNRVLEKIADELEAQSEIILNANAQDVADARANGLSE 60 ++E + A QA+ LAQ+ ++ KN +L +A L S I +AN D+A A GLS Sbjct: 3 IIETLSRDAAQAAKTLAQVDTQTKNTILLDMARSLRDNSFEIRSANLIDLASAEQAGLSH 62 Query: 61 AMLDRLALTPARLKGIADDVRQVCNLADPVGQVIDGGVLDSGLRLERRRVPLGVIGVIYE 120 AM+DRL L R++ +A + + L DP+G D +GL + + RVPLGV+ +IYE Sbjct: 63 AMIDRLTLDGDRIEAMAHGIEIIATLPDPIGVQRDLSTRPNGLAISKMRVPLGVVCMIYE 122 Query: 121 ARPNVTVDVASLCLKTGNAVILRGGKETCRTNAATVAVIQDALKSCGLPAGAVQAIDNPD 180 ARPNVT D +LC K+GNAVILRGGKE T+ +V+Q LK GLPA + + +PD Sbjct: 123 ARPNVTADAGALCFKSGNAVILRGGKEALHTSKVIASVLQKVLKQYGLPASLIAVVPDPD 182 Query: 181 RALVSEMLRMDKYIDMLIPRGGAGLHKLCREQSTIPVITGGIGVCHIYVDESVEIAEALK 240 RAL+ E+++ ID++IPRGG GL E S +PVI GVCH+YVD+ ++ +AL Sbjct: 183 RALLMELMQQRDTIDVIIPRGGEGLINFVTEHSKVPVIQHFKGVCHLYVDKDADLDKALA 242 Query: 241 VIVNAKTQRPSTCNTVETLLVNKNIADSFLPALSKQMAESGVTLHADAAALAQLQAGPAK 300 +++N KTQR CN +E LLV+ +A FL + +A+ V ++ A Q A Sbjct: 243 LLLNGKTQRTGVCNALEGLLVHSEVAPKFLAMAATALAKHQVKIN----CCANTQQYFAA 298 Query: 301 VVAVKAEEYDDEFLSLDLNVKIVSDLDDAIAHIREHGTQHSDAILTRDMRNAQRFVNEVD 360 + EE+ E+L L+L V+ V D D A+AHI G++H++ I T + A+RF VD Sbjct: 299 AQVLSDEEFGQEYLDLELAVRQVKDFDQAVAHIHRFGSRHTEVICTENELTAKRFQRTVD 358 Query: 361 SSAVYVNASTRFTDGGQFGLGAEVAVSTQKLHARGPMGLEALTTYKWIGIGDYTIRA 417 +S V VNAS+RF+DGG+ GLGAE+ ++T KLHA GPMGLE+LTT K++ GD IRA Sbjct: 359 ASVVMVNASSRFSDGGELGLGAEIGIATTKLHAYGPMGLESLTTEKYLVNGDGQIRA 415 Lambda K H 0.317 0.133 0.369 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: 405 Number of extensions: 17 Number of successful extensions: 2 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: 417 Length of database: 415 Length adjustment: 31 Effective length of query: 386 Effective length of database: 384 Effective search space: 148224 Effective search space used: 148224 Neighboring words threshold: 11 Window for multiple hits: 40 X1: 16 ( 7.3 bits) X2: 38 (14.6 bits) X3: 64 (24.7 bits) S1: 41 (21.7 bits) S2: 50 (23.9 bits)
Align candidate 5210587 Shew_3015 (gamma-glutamyl phosphate reductase (RefSeq))
to HMM TIGR00407 (proA: glutamate-5-semialdehyde dehydrogenase (EC 1.2.1.41))
# 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/TIGR00407.hmm # target sequence database: /tmp/gapView.20248.genome.faa # - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - Query: TIGR00407 [M=398] Accession: TIGR00407 Description: proA: glutamate-5-semialdehyde dehydrogenase 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 ------- ------ ----- ------- ------ ----- ---- -- -------- ----------- 5e-140 452.7 1.7 5.8e-140 452.5 1.7 1.0 1 lcl|FitnessBrowser__PV4:5210587 Shew_3015 gamma-glutamyl phospha Domain annotation for each sequence (and alignments): >> lcl|FitnessBrowser__PV4:5210587 Shew_3015 gamma-glutamyl phosphate reductase (RefSeq) # score bias c-Evalue i-Evalue hmmfrom hmm to alifrom ali to envfrom env to acc --- ------ ----- --------- --------- ------- ------- ------- ------- ------- ------- ---- 1 ! 452.5 1.7 5.8e-140 5.8e-140 1 398 [] 11 404 .. 11 404 .. 0.98 Alignments for each domain: == domain 1 score: 452.5 bits; conditional E-value: 5.8e-140 TIGR00407 1 akeaalklaqlstaeknealskiadeLkaeaelilaanakdiaaakenGladalldrLlLteeklksiaddvkdvieL 78 a +aa +laq+ t+ kn++l +a +L+ ++ +i an +d+a+a++ Gl++a++drL+L+ ++++ +a++++ ++ L lcl|FitnessBrowser__PV4:5210587 11 AAQAAKTLAQVDTQTKNTILLDMARSLRDNSFEIRSANLIDLASAEQAGLSHAMIDRLTLDGDRIEAMAHGIEIIATL 88 679*************************************************************************** PP TIGR00407 79 adPvGkvieareldeGLklervrvPlGvlgviyearPevivdvasLclktGnaviLkGgkeavrsnkalveviqdale 156 +dP+G + ++ +GL + ++rvPlGv+ +iyearP+v++d+ +Lc+k+GnaviL+Ggkea ++ k++++v+q+ l+ lcl|FitnessBrowser__PV4:5210587 89 PDPIGVQRDLSTRPNGLAISKMRVPLGVVCMIYEARPNVTADAGALCFKSGNAVILRGGKEALHTSKVIASVLQKVLK 166 ****************************************************************************** PP TIGR00407 157 qtglpveavqliedpdreevkellkldeyvdlliPrGgnelvklikeestiPvlehadGvChiyldesadlakakkvi 234 q glp+ + ++ dpdr+ ++el+++ + +d++iPrGg++l++ + e+s++Pv++h +GvCh+y+d++adl ka + lcl|FitnessBrowser__PV4:5210587 167 QYGLPASLIAVVPDPDRALLMELMQQRDTIDVIIPRGGEGLINFVTEHSKVPVIQHFKGVCHLYVDKDADLDKALALL 244 ****************************************************************************** PP TIGR00407 235 vdaktqrPstCnaietLLvnkaiaeefleeLekqleekgvelradalvlkllelekateaevskedfdkeflsldLsv 312 ++ ktqr +Cna+e LLv+ ++a +fl + +l+++ v+++ a +++ ++ + s+e+f +e+l+l L+v lcl|FitnessBrowser__PV4:5210587 245 LNGKTQRTGVCNALEGLLVHSEVAPKFLAMAATALAKHQVKINCCANTQQYFAAA--Q--VLSDEEFGQEYLDLELAV 318 *******************************************999998887776..3..366899************ PP TIGR00407 313 kivedleeaiehirqygtkhsdailtedkknaekfvkevdsaavyvnastrfadGfrfGfGaevgistqklharGPvG 390 + v+d ++a++hi+++g++h++ i te++ +a++f+++vd++ v vnas rf+dG++ G+Gae+gi+t klha GP+G lcl|FitnessBrowser__PV4:5210587 319 RQVKDFDQAVAHIHRFGSRHTEVICTENELTAKRFQRTVDASVVMVNASSRFSDGGELGLGAEIGIATTKLHAYGPMG 396 ****************************************************************************** PP TIGR00407 391 LeaLvsyk 398 Le+L++ k lcl|FitnessBrowser__PV4:5210587 397 LESLTTEK 404 *****976 PP Internal pipeline statistics summary: ------------------------------------- Query model(s): 1 (398 nodes) Target sequences: 1 (415 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: 10.56 // [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