Align Gamma-glutamyl phosphate reductase; GPR; Glutamate-5-semialdehyde dehydrogenase; Glutamyl-gamma-semialdehyde dehydrogenase; GSA dehydrogenase; EC 1.2.1.41 (characterized)
to candidate BPHYT_RS16770 BPHYT_RS16770 gamma-glutamyl phosphate reductase
Query= SwissProt::P07004 (417 letters) >FitnessBrowser__BFirm:BPHYT_RS16770 Length = 423 Score = 368 bits (945), Expect = e-106 Identities = 192/411 (46%), Positives = 271/411 (65%), Gaps = 1/411 (0%) Query: 2 LEQMGIAAKQASYKLAQLSSREKNRVLEKIADELEAQSEIILNANAQDVADARANGLSEA 61 + +G A+QAS +A+ S+ KN L +A +E + ++ ANA+DVA AR G A Sbjct: 7 MTDLGRRARQASRAMARASTAAKNAALAAVAQGIERDAALLKEANARDVARAREKGHDAA 66 Query: 62 MLDRLALTPARLKGIADDVRQVCNLADPVGQVIDGGVLDSGLRLERRRVPLGVIGVIYEA 121 +DRL L+ LK + + +RQV LADP+G++ + SG+++ + RVPLGVIG+IYE+ Sbjct: 67 FIDRLTLSDKALKTMVEGLRQVAALADPIGEISNLKYRPSGIQVGQMRVPLGVIGIIYES 126 Query: 122 RPNVTVDVASLCLKTGNAVILRGGKETCRTNAATVAVIQDALKSCGLPAGAVQAIDNPDR 181 RPNVT+D A+LCLK+GNA ILRGG E NAA +I + L+ GLP AVQ + DR Sbjct: 127 RPNVTIDAAALCLKSGNATILRGGSEALECNAALAKLIGEGLEKAGLPQEAVQVVATSDR 186 Query: 182 ALVSEMLRMDKYIDMLIPRGGAGLHKLCREQSTIPVITGGIGVCHIYVDESVEIAEALKV 241 A V +++ M +Y+D+++PRGG L + ++ +P+I G+CH+YVD+ ++A+AL V Sbjct: 187 AAVGKLITMTEYVDVIVPRGGKSLIERLMNEARVPMIKHLDGICHVYVDDRADLAKALTV 246 Query: 242 IVNAKTQRPSTCNTVETLLVNKNIADSFLPALSKQMAESGVTLHADAAALAQL-QAGPAK 300 NAKT R TCNT+ETLLV + IA LP L K + V L DAAA A L AG Sbjct: 247 CDNAKTHRYGTCNTMETLLVARGIAAEVLPPLGKLYRDKQVELRVDAAARAVLADAGVGP 306 Query: 301 VVAVKAEEYDDEFLSLDLNVKIVSDLDDAIAHIREHGTQHSDAILTRDMRNAQRFVNEVD 360 +V E++ E+L+ L +K+V +LD AI HI + +QH+DAI+T D A RF+ EVD Sbjct: 307 LVDATEEDWRTEYLAPVLAIKVVENLDAAIDHINTYSSQHTDAIVTEDHDRAMRFLREVD 366 Query: 361 SSAVYVNASTRFTDGGQFGLGAEVAVSTQKLHARGPMGLEALTTYKWIGIG 411 S++V VNASTRF DG +FGLGAE+ +S KLHARGP+GLE LT+ K++ +G Sbjct: 367 SASVMVNASTRFADGFEFGLGAEIGISNDKLHARGPVGLEGLTSLKYVVLG 417 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: 421 Number of extensions: 18 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: 423 Length adjustment: 32 Effective length of query: 385 Effective length of database: 391 Effective search space: 150535 Effective search space used: 150535 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 BPHYT_RS16770 BPHYT_RS16770 (gamma-glutamyl phosphate reductase)
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.8451.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 ------- ------ ----- ------- ------ ----- ---- -- -------- ----------- 9e-155 501.3 2.6 1e-154 501.1 2.6 1.0 1 lcl|FitnessBrowser__BFirm:BPHYT_RS16770 BPHYT_RS16770 gamma-glutamyl pho Domain annotation for each sequence (and alignments): >> lcl|FitnessBrowser__BFirm:BPHYT_RS16770 BPHYT_RS16770 gamma-glutamyl phosphate reductase # score bias c-Evalue i-Evalue hmmfrom hmm to alifrom ali to envfrom env to acc --- ------ ----- --------- --------- ------- ------- ------- ------- ------- ------- ---- 1 ! 501.1 2.6 1e-154 1e-154 1 398 [] 14 412 .. 14 412 .. 0.98 Alignments for each domain: == domain 1 score: 501.1 bits; conditional E-value: 1e-154 TIGR00407 1 akeaalklaqlstaeknealskiadeLkaeaelilaanakdiaaakenGladalldrLlLteeklksiad 70 a++a+ +a sta kn al+++a++++++a l+ +ana+d+a a+e+G a++drL+L+++ lk++++ lcl|FitnessBrowser__BFirm:BPHYT_RS16770 14 ARQASRAMARASTAAKNAALAAVAQGIERDAALLKEANARDVARAREKGHDAAFIDRLTLSDKALKTMVE 83 89******************************************************************** PP TIGR00407 71 dvkdvieLadPvGkvieareldeGLklervrvPlGvlgviyearPevivdvasLclktGnaviLkGgkea 140 ++++v+ LadP+G++ + + + +G+++ ++rvPlGv+g+iye+rP+v++d+a+Lclk+Gna iL+Gg+ea lcl|FitnessBrowser__BFirm:BPHYT_RS16770 84 GLRQVAALADPIGEISNLKYRPSGIQVGQMRVPLGVIGIIYESRPNVTIDAAALCLKSGNATILRGGSEA 153 ********************************************************************** PP TIGR00407 141 vrsnkalveviqdaleqtglpveavqliedpdreevkellkldeyvdlliPrGgnelvklikeestiPvl 210 + n+al+++i + le++glp+eavq++ ++dr+ v +l+++ eyvd+++PrGg++l++ + +e+++P++ lcl|FitnessBrowser__BFirm:BPHYT_RS16770 154 LECNAALAKLIGEGLEKAGLPQEAVQVVATSDRAAVGKLITMTEYVDVIVPRGGKSLIERLMNEARVPMI 223 ********************************************************************** PP TIGR00407 211 ehadGvChiyldesadlakakkvivdaktqrPstCnaietLLvnkaiaeefleeLekqleekgvelrada 280 +h dG+Ch+y+d+ adlaka +v ++akt+r tCn++etLLv + ia+e l+ L k +k velr da lcl|FitnessBrowser__BFirm:BPHYT_RS16770 224 KHLDGICHVYVDDRADLAKALTVCDNAKTHRYGTCNTMETLLVARGIAAEVLPPLGKLYRDKQVELRVDA 293 *********************************************************************9 PP TIGR00407 281 lvlkll.elekateaevskedfdkeflsldLsvkivedleeaiehirqygtkhsdailtedkknaekfvk 349 ++ ++l +++ +++++ed+++e+l+++L++k+ve+l++ai+hi++y+++h+dai+ted+ a +f++ lcl|FitnessBrowser__BFirm:BPHYT_RS16770 294 AARAVLaDAGVGPLVDATEEDWRTEYLAPVLAIKVVENLDAAIDHINTYSSQHTDAIVTEDHDRAMRFLR 363 9988761555567899****************************************************** PP TIGR00407 350 evdsaavyvnastrfadGfrfGfGaevgistqklharGPvGLeaLvsyk 398 evdsa+v vnastrfadGf+fG+Gae+gis +klharGPvGLe+L+s k lcl|FitnessBrowser__BFirm:BPHYT_RS16770 364 EVDSASVMVNASTRFADGFEFGLGAEIGISNDKLHARGPVGLEGLTSLK 412 **********************************************976 PP Internal pipeline statistics summary: ------------------------------------- Query model(s): 1 (398 nodes) Target sequences: 1 (423 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: 10.73 // [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