Align succinyldiaminopimelate transaminase (EC 2.6.1.17) (characterized)
to candidate RR42_RS11930 RR42_RS11930 succinyldiaminopimelate aminotransferase
Query= BRENDA::Q9ZEX3 (397 letters) >lcl|FitnessBrowser__Cup4G11:RR42_RS11930 RR42_RS11930 succinyldiaminopimelate aminotransferase Length = 405 Score = 468 bits (1203), Expect = e-136 Identities = 245/404 (60%), Positives = 287/404 (71%), Gaps = 10/404 (2%) Query: 1 MNPRLDALHPYPFEKLRALLADAGKPTHDLPPINLSIGEPKHAAPACVGQAIAANLAGLS 60 MNPRLD L PYPFEKLR LLAD KP LP I+ IGEPKH P + A++ L GL+ Sbjct: 1 MNPRLDLLQPYPFEKLRVLLADV-KPNGALPAISFGIGEPKHPTPEFIKTALSNALQGLA 59 Query: 61 VYPSTKGEPALRQAISQWLSRRYSIPAPDPESEVLPVLGSREALFAFAQTVIDPSA-GAL 119 YP+T G ALRQ ++ W+ RRY++PA + ++VLPV GSREALFAFAQTV+D S GAL Sbjct: 60 NYPTTAGSDALRQCMAAWIQRRYNLPAVNATTQVLPVTGSREALFAFAQTVVDASQPGAL 119 Query: 120 VVCPNPFYQIYEGAALLAGATPYYVNADPARDFGLRTGRVPDEVWRRTQLVFVCSPGNPA 179 V+CPNPFYQIYEGAALLAGATP + N+DPAR+F R+ E W + QLVFVCSPGNP Sbjct: 120 VLCPNPFYQIYEGAALLAGATPVFANSDPARNFAPAFDRIGAETWAKVQLVFVCSPGNPT 179 Query: 180 GNVMSLEEWRTLFELSDRHGFVIAAYECYSEIYLDEDTPPLGSLQAARRLGRDR----YT 235 G V+SLE+WR LF LSDRHGFVIA+ ECYSEIY E PPLG+L+AA +LGR + Sbjct: 180 GAVLSLEDWRELFALSDRHGFVIASDECYSEIYFKEGEPPLGALEAAHKLGRAEGAHPFE 239 Query: 236 NLVAFSSLSKRSNVPGMRSGFVAGDAALLARFLLYRTYHGSAMSPVVSAASIAAWSMRRM 295 LV FSSLSKRSNVPG+RSGFVAGDAALL +FLLYRTYHG AM+P V AS+AAW+ Sbjct: 240 RLVMFSSLSKRSNVPGLRSGFVAGDAALLKKFLLYRTYHGGAMNPAVQTASVAAWNDEAH 299 Query: 296 CRKT-AQYRAKFEAVLPILQNVLDVRAPQASFYLWAG---TPGSDTAFARELYGRTGVTV 351 R A Y KF V P+L VLDV P A FYLWA T SDT FA L VTV Sbjct: 300 VRNNRAAYARKFAEVTPMLAEVLDVALPDAGFYLWADVSRTGLSDTEFAARLLAEQNVTV 359 Query: 352 LPGSLLAREAHNANPGQGRIRIALVAPLDQCVQAAERIAHFART 395 LPGS LAREA NPG R+R+ALVA ++C++ A RI F ++ Sbjct: 360 LPGSYLAREADGINPGANRVRMALVATPEECLEGARRIVAFCKS 403 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: 569 Number of extensions: 22 Number of successful extensions: 6 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: 405 Length adjustment: 31 Effective length of query: 366 Effective length of database: 374 Effective search space: 136884 Effective search space used: 136884 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 RR42_RS11930 RR42_RS11930 (succinyldiaminopimelate aminotransferase)
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.11866.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 ------- ------ ----- ------- ------ ----- ---- -- -------- ----------- 2.8e-184 598.4 0.0 3.2e-184 598.3 0.0 1.0 1 lcl|FitnessBrowser__Cup4G11:RR42_RS11930 RR42_RS11930 succinyldiaminopime Domain annotation for each sequence (and alignments): >> lcl|FitnessBrowser__Cup4G11:RR42_RS11930 RR42_RS11930 succinyldiaminopimelate aminotransferase # score bias c-Evalue i-Evalue hmmfrom hmm to alifrom ali to envfrom env to acc --- ------ ----- --------- --------- ------- ------- ------- ------- ------- ------- ---- 1 ! 598.3 0.0 3.2e-184 3.2e-184 1 395 [] 1 401 [. 1 401 [. 0.98 Alignments for each domain: == domain 1 score: 598.3 bits; conditional E-value: 3.2e-184 TIGR03538 1 mnpnlerlkpyPfeklaellkdvtppadleeialsiGePkhatPafvlealvenleelskyPttkGlpe 69 mnp+l+ l+pyPfekl+ ll+dv+p+ l++i++ iGePkh+tP+f++ al + l++l++yPtt+G+++ lcl|FitnessBrowser__Cup4G11:RR42_RS11930 1 MNPRLDLLQPYPFEKLRVLLADVKPNGALPAISFGIGEPKHPTPEFIKTALSNALQGLANYPTTAGSDA 69 9******************************************************************** PP TIGR03538 70 lreaiaeWlerrfelpagvdperqvlPvnGtrealfafvqavidrae.kalvvlPnPfyqiyeGaalla 137 lr+++a+W++rr++lpa v++ +qvlPv+G+realfaf+q+v+d ++ alv++PnPfyqiyeGaalla lcl|FitnessBrowser__Cup4G11:RR42_RS11930 70 LRQCMAAWIQRRYNLPA-VNATTQVLPVTGSREALFAFAQTVVDASQpGALVLCPNPFYQIYEGAALLA 137 *****************.**************************9997899****************** PP TIGR03538 138 gaepyflnctaengfkpdfdavpeevWkrvqllfvcsPgnPtGavlsleelkklleladkydfiiasde 206 ga+p+f n++++ +f p fd + +e+W++vql+fvcsPgnPtGavlsle++++l++l+d+++f+iasde lcl|FitnessBrowser__Cup4G11:RR42_RS11930 138 GATPVFANSDPARNFAPAFDRIGAETWAKVQLVFVCSPGNPTGAVLSLEDWRELFALSDRHGFVIASDE 206 ********************************************************************* PP TIGR03538 207 cyselyldeaeaPvGlleaaaelGrdd....fkrllvfhslskrsnvPGlrsGfvaGdaellkeflryr 271 cyse+y+ e e+P+G leaa++lGr + f+rl++f+slskrsnvPGlrsGfvaGda+llk+fl yr lcl|FitnessBrowser__Cup4G11:RR42_RS11930 207 CYSEIYFKEGEPPLGALEAAHKLGRAEgahpFERLVMFSSLSKRSNVPGLRSGFVAGDAALLKKFLLYR 275 ***********************996544449************************************* PP TIGR03538 272 tyhGcampiavqlasiaaWedekhvrenralyrekfaavleilgavldlelPdasfylWlkv..pdgdd 338 tyhG am++avq+as+aaW+de+hvr+nra+y++kfa v+ +l++vld+ lPda+fylW+ v + d lcl|FitnessBrowser__Cup4G11:RR42_RS11930 276 TYHGGAMNPAVQTASVAAWNDEAHVRNNRAAYARKFAEVTPMLAEVLDVALPDAGFYLWADVsrTGLSD 344 ************************************************************99544679* PP TIGR03538 339 eafaralyeeenvkvlpGrylsreaegvnPGegrvrlalvaeleecveaaerikkll 395 ++fa +l +e+nv+vlpG+yl+rea+g nPG++rvr+alva eec e+a+ri +++ lcl|FitnessBrowser__Cup4G11:RR42_RS11930 345 TEFAARLLAEQNVTVLPGSYLAREADGINPGANRVRMALVATPEECLEGARRIVAFC 401 *****************************************************9885 PP Internal pipeline statistics summary: ------------------------------------- Query model(s): 1 (395 nodes) Target sequences: 1 (405 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: 10.30 // [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