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.6768.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: 0.00u 0.01s 00:00:00.01 Elapsed: 00:00:00.01 # Mc/sec: 12.51 // [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