Align 4-aminobutyrate-2-oxoglutarate transaminase (EC 2.6.1.19) (characterized)
to candidate SM_b21186 SM_b21186 4-aminobutyrate aminotransferase
Query= BRENDA::Q0K2K2 (423 letters) >FitnessBrowser__Smeli:SM_b21186 Length = 422 Score = 544 bits (1401), Expect = e-159 Identities = 267/416 (64%), Positives = 316/416 (75%) Query: 8 LNQRRTLATPRGVGVMCDFYADRAENATLWDVEGRAYTDFAAGIAVLNTGHRHPRVMQAI 67 L R+ A RGVG+ YADRAENA +WD EG Y DFAAGIAV+NTGHRHP+V+ A+ Sbjct: 4 LTDRKNAAISRGVGMTTQVYADRAENAEIWDKEGNRYIDFAAGIAVVNTGHRHPKVIAAV 63 Query: 68 AAQLERFTHTAYQIVPYQGYVTLAERINALVPIQGLNKTALFTTGAEAVENAIKIARAHT 127 AQL+RFTHT +Q+VPY+ YV LAER+NA+VP KT TTGAEAVENA+KIARA T Sbjct: 64 KAQLDRFTHTCHQVVPYENYVHLAERLNAIVPGDFAKKTIFVTTGAEAVENAVKIARAAT 123 Query: 128 GRPGVIAFSGAFHGRTLLGMALTGKVAPYKIGFGPFPSDIYHAPFPSALHGVSTERALQA 187 GR V+AF G FHGRT +GMALTGKV PYK+GFG P+D++HAPFP LHGV+ E++L A Sbjct: 124 GRQAVVAFGGGFHGRTFMGMALTGKVVPYKVGFGAMPADVFHAPFPIELHGVTVEQSLSA 183 Query: 188 LEGLFKTDIDPARVAAIIVEPVQGEGGFQAAPADFMRGLRAVCDQHGIVLIADEVQTGFG 247 L+ LF D+DPARVAAII+EPVQGEGGF P FM+ LR VCDQHGI+LIADEVQTGF Sbjct: 184 LKKLFAADVDPARVAAIIIEPVQGEGGFYPVPTAFMKALREVCDQHGILLIADEVQTGFA 243 Query: 248 RTGKMFAMSHHDVEPDLITMAKSLAGGMPLSAVSGRAAIMDAPLPGGLGGTYAGNPLAVA 307 RTGK+FAM HH V PDL TMAKSLAGG PL+AV+GRA IMDAP PGGLGGTY GNPL +A Sbjct: 244 RTGKLFAMEHHGVAPDLTTMAKSLAGGFPLAAVTGRAEIMDAPGPGGLGGTYGGNPLGIA 303 Query: 308 AAHAVIDVIEEEKLCERSASLGQQLREHLLAQRKHCPAMAEVRGLGSMVAAEFCDPATGQ 367 AAHAV+DVI EE LCER+ LG +L++ L A R+ P + ++RG G M A EF D T Sbjct: 304 AAHAVLDVIAEENLCERANQLGNRLKQRLAAIREKAPEIVDIRGPGFMNAVEFNDVRTNL 363 Query: 368 PSAEHAKRVQTRALEAGLVLLTCGTYGNVIRFLYPLTIPQAQFDAALAVLTQALAE 423 PSAE A +V+ ALE GL+LLTCG +GNVIRFL P+TI F AL + ++ E Sbjct: 364 PSAEFANKVRLLALEKGLILLTCGVHGNVIRFLAPITIQDEVFAEALDTIEASILE 419 Lambda K H 0.321 0.136 0.400 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: 603 Number of extensions: 17 Number of successful extensions: 1 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: 423 Length of database: 422 Length adjustment: 32 Effective length of query: 391 Effective length of database: 390 Effective search space: 152490 Effective search space used: 152490 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 SM_b21186 SM_b21186 (4-aminobutyrate aminotransferase)
to HMM TIGR00700 (gabT: 4-aminobutyrate transaminase (EC 2.6.1.19))
# 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.carbon/TIGR00700.hmm # target sequence database: /tmp/gapView.21361.genome.faa # - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - Query: TIGR00700 [M=420] Accession: TIGR00700 Description: GABAtrnsam: 4-aminobutyrate 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 ------- ------ ----- ------- ------ ----- ---- -- -------- ----------- 3.2e-184 598.3 6.6 3.9e-184 598.0 6.6 1.0 1 lcl|FitnessBrowser__Smeli:SM_b21186 SM_b21186 4-aminobutyrate aminot Domain annotation for each sequence (and alignments): >> lcl|FitnessBrowser__Smeli:SM_b21186 SM_b21186 4-aminobutyrate aminotransferase # score bias c-Evalue i-Evalue hmmfrom hmm to alifrom ali to envfrom env to acc --- ------ ----- --------- --------- ------- ------- ------- ------- ------- ------- ---- 1 ! 598.0 6.6 3.9e-184 3.9e-184 2 418 .. 7 417 .. 6 419 .. 0.98 Alignments for each domain: == domain 1 score: 598.0 bits; conditional E-value: 3.9e-184 TIGR00700 2 rraaavskGvgvtlrvlaakaegaelkdvdGnrlidlaagiavlnvGhshPkvveavkrqveelthtafqvvpy 75 r++aa+s+Gvg+t++v+a +ae+ae+ d +Gnr+id+aagiav+n+Gh+hPkv++avk q++++tht++qvvpy lcl|FitnessBrowser__Smeli:SM_b21186 7 RKNAAISRGVGMTTQVYADRAENAEIWDKEGNRYIDFAAGIAVVNTGHRHPKVIAAVKAQLDRFTHTCHQVVPY 80 7899********************************************************************** PP TIGR00700 76 esyvelaeklnaiaPgsgekkavllnsGaeavenavkiarkytgrpgvvafsrgfhGrtnltmaltakvkPyki 149 e yv+lae+lnai Pg kk++++++Gaeavenavkiar+ tgr++vvaf +gfhGrt++ malt+kv Pyk+ lcl|FitnessBrowser__Smeli:SM_b21186 81 ENYVHLAERLNAIVPGDFAKKTIFVTTGAEAVENAVKIARAATGRQAVVAFGGGFHGRTFMGMALTGKVVPYKV 154 ************************************************************************** PP TIGR00700 150 GfGPfapevyraPlpydyrdialdkqeslddelaaiealfvadveaeqvaavvlePvqGeGGfivpakelvaav 223 GfG ++++v++aP+p ++++ ++ ++s l+a+++lf adv++ +vaa+++ePvqGeGGf + +++a+ lcl|FitnessBrowser__Smeli:SM_b21186 155 GFGAMPADVFHAPFPIELHGVTV--EQS----LSALKKLFAADVDPARVAAIIIEPVQGEGGFYPVPTAFMKAL 222 *******************9988..445....55**************************************** PP TIGR00700 224 aslckehgivliadevqtGfartGklfaieheddkPdlitvaksladGlPlsgvvGraeildapapGglGGtya 297 +++c++hgi+liadevqtGfartGklfa+eh+++ Pdl t+aksla+G+Pl++v+Graei+dap pGglGGty+ lcl|FitnessBrowser__Smeli:SM_b21186 223 REVCDQHGILLIADEVQTGFARTGKLFAMEHHGVAPDLTTMAKSLAGGFPLAAVTGRAEIMDAPGPGGLGGTYG 296 ************************************************************************** PP TIGR00700 298 GnPlavaaalavldiieeeglieraeqigklvkdklielkeevpaigdvrglGamiavelvdpdttePdaalae 371 GnPl++aaa+avld+i ee l+era+q+g+++k++l ++e+ p i d+rg G m ave++d t+ P+a a+ lcl|FitnessBrowser__Smeli:SM_b21186 297 GNPLGIAAAHAVLDVIAEENLCERANQLGNRLKQRLAAIREKAPEIVDIRGPGFMNAVEFNDVRTNLPSAEFAN 370 ************************************************************************** PP TIGR00700 372 kiaaaalaaGlllltaGifGniirlltPltisdelldeglkileaal 418 k+ al++Gl+llt+G++Gn+ir+l+P+ti de + e+l+ +ea++ lcl|FitnessBrowser__Smeli:SM_b21186 371 KVRLLALEKGLILLTCGVHGNVIRFLAPITIQDEVFAEALDTIEASI 417 *****************************************999865 PP Internal pipeline statistics summary: ------------------------------------- Query model(s): 1 (420 nodes) Target sequences: 1 (422 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 0.00s 00:00:00.01 Elapsed: 00:00:00.01 # Mc/sec: 9.17 // [ok]
This GapMind analysis is from Sep 17 2021. The underlying query database was built on Sep 17 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.
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