Align thymidine phosphorylase (EC 2.4.2.4) (characterized)
to candidate SMc04122 SMc04122 thymidine phosphorylase
Query= BRENDA::P07650 (440 letters) >FitnessBrowser__Smeli:SMc04122 Length = 440 Score = 444 bits (1143), Expect = e-129 Identities = 237/436 (54%), Positives = 297/436 (68%), Gaps = 2/436 (0%) Query: 3 LAQEIIRKKRDGHALSDEEIRFFINGIRDNTISEGQIAALAMTIFFHDMTMPERVSLTMA 62 L QEIIRKKRDG L EI FI G+ D ++SEGQ AA AM ++F M E V+LT+A Sbjct: 4 LPQEIIRKKRDGDRLDPAEIAGFIAGVTDGSVSEGQAAAFAMAVWFSGMNRDECVALTLA 63 Query: 63 MRDSGTVLDWKSLHLNGPIVDKHSTGGVGDVTSLMLGPMVAACGGYIPMISGRGLGHTGG 122 MRDSG LDW L PIVDKHSTGGVGD SLML P+VAACG +PMISGRGLGHTGG Sbjct: 64 MRDSGETLDWSDLAR--PIVDKHSTGGVGDNVSLMLAPIVAACGAAVPMISGRGLGHTGG 121 Query: 123 TLDKLESIPGFDIFPDDNRFREIIKDVGVAIIGQTSSLAPADKRFYATRDITATVDSIPL 182 TLDKLESIPG+DI P FR + +VG AIIGQT+ LAPADKR YA RD+TATVDS+PL Sbjct: 122 TLDKLESIPGYDIQPSPELFRRVADEVGCAIIGQTADLAPADKRLYAIRDVTATVDSVPL 181 Query: 183 ITASILAKKLAEGLDALVMDVKVGSGAFMPTYELSEALAEAIVGVANGAGVRTTALLTDM 242 ITASIL+KKLA GL +LV+DVK+G+G+FM +E LA ++V VANGAGVRT+AL+TDM Sbjct: 182 ITASILSKKLAAGLRSLVLDVKLGNGSFMTDPAETEVLARSLVEVANGAGVRTSALITDM 241 Query: 243 NQVLASSAGNAVEVREAVQFLTGEYRNPRLFDVTMALCVEMLISGKLAKDDAEARAKLQA 302 N+ LA +AGNA+E+ + +L GE RL V MAL EML++ +A +AEA A + Sbjct: 242 NEPLADAAGNALEIENCLAYLRGEKAGTRLDQVVMALAAEMLVAAGIAAHEAEAEAMARR 301 Query: 303 VLDNGKAAEVFGRMVAAQKGPTDFVENYAKYLPTAMLTKAVYADTEGFVSEMDTRALGMA 362 VL +G+A E FG MV GP DFV+ YL A AV A G+++ TR LGMA Sbjct: 302 VLGSGEAMERFGLMVHRLGGPADFVDRPGAYLAKAPAILAVPAGRHGYLTSCKTRELGMA 361 Query: 363 VVAMGGGRRQASDTIDYSVGFTDMARLGDQVDGQRPLAVIHAKDENNWQEAAKAVKAAIK 422 V+ +GGGR + D ID+ VG T + LG +V+ P+A +HA D++ + AK V Sbjct: 362 VIELGGGRIRPDDRIDHRVGLTGLRPLGTKVEKGEPIAFVHAADQSQAEAIAKRVVTLYA 421 Query: 423 LADKAPESTPTVYRRI 438 +AD+ P P + ++ Sbjct: 422 IADEEPARRPVIVSKL 437 Lambda K H 0.318 0.134 0.377 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: 505 Number of extensions: 22 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: 440 Length of database: 440 Length adjustment: 32 Effective length of query: 408 Effective length of database: 408 Effective search space: 166464 Effective search space used: 166464 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 (21.7 bits) S2: 51 (24.3 bits)
Align candidate SMc04122 SMc04122 (thymidine phosphorylase)
to HMM TIGR02643 (deoA: thymidine phosphorylase (EC 2.4.2.4))
# 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/TIGR02643.hmm # target sequence database: /tmp/gapView.4067.genome.faa # - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - Query: TIGR02643 [M=437] Accession: TIGR02643 Description: T_phosphoryl: thymidine phosphorylase 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 ------- ------ ----- ------- ------ ----- ---- -- -------- ----------- 3.1e-234 763.6 6.9 3.5e-234 763.4 6.9 1.0 1 lcl|FitnessBrowser__Smeli:SMc04122 SMc04122 thymidine phosphorylase Domain annotation for each sequence (and alignments): >> lcl|FitnessBrowser__Smeli:SMc04122 SMc04122 thymidine phosphorylase # score bias c-Evalue i-Evalue hmmfrom hmm to alifrom ali to envfrom env to acc --- ------ ----- --------- --------- ------- ------- ------- ------- ------- ------- ---- 1 ! 763.4 6.9 3.5e-234 3.5e-234 1 436 [. 3 436 .. 3 437 .. 1.00 Alignments for each domain: == domain 1 score: 763.4 bits; conditional E-value: 3.5e-234 TIGR02643 1 llpqeiirkkrdglslsdeeiaafvegvtddsvsegqiaalamavyfngleldekvaltlamrdsGdvldwkdld 75 +lpqeiirkkrdg++l+++eia f++gvtd+svsegq+aa+amav+f+g+++de+valtlamrdsG++ldw+ d lcl|FitnessBrowser__Smeli:SMc04122 3 MLPQEIIRKKRDGDRLDPAEIAGFIAGVTDGSVSEGQAAAFAMAVWFSGMNRDECVALTLAMRDSGETLDWS--D 75 89**********************************************************************..* PP TIGR02643 76 lngPvvdkhstGGvGdvvslmlaPivaacGgyvPmisGrGlGhtGGtldkleaiPGydvaPdeelfrkvvkdvGv 150 l++P+vdkhstGGvGd+vslmlaPivaacG++vPmisGrGlGhtGGtldkle+iPGyd++P++elfr+v+++vG+ lcl|FitnessBrowser__Smeli:SMc04122 76 LARPIVDKHSTGGVGDNVSLMLAPIVAACGAAVPMISGRGLGHTGGTLDKLESIPGYDIQPSPELFRRVADEVGC 150 *************************************************************************** PP TIGR02643 151 aiiGqtadlaPadkrlyairdvtatvesiplitasilskklaaGldalvldvkvGnGafmesleeseelarslve 225 aiiGqtadlaPadkrlyairdvtatv+s+plitasilskklaaGl++lvldvk+GnG+fm++ +e+e+larslve lcl|FitnessBrowser__Smeli:SMc04122 151 AIIGQTADLAPADKRLYAIRDVTATVDSVPLITASILSKKLAAGLRSLVLDVKLGNGSFMTDPAETEVLARSLVE 225 *************************************************************************** PP TIGR02643 226 vangaGvrttalitdmnqalasaaGnavevreavdfltGekrdkrleevtlalaaellvsgklaadeaeaeakle 300 vangaGvrt+alitdmn++la+aaGna+e+++++++l+Gek+++rl++v++alaae+lv++++aa+eaeaea+++ lcl|FitnessBrowser__Smeli:SMc04122 226 VANGAGVRTSALITDMNEPLADAAGNALEIENCLAYLRGEKAGTRLDQVVMALAAEMLVAAGIAAHEAEAEAMAR 300 *************************************************************************** PP TIGR02643 301 avlesGraaerfarmvaalgGPadfvekpekylakaaiakavkaaregylseidtrelGlavvalGGGrrkaddk 375 +vl+sG+a+erf+ mv++lgGPadfv++p +ylaka++++av+a r+gyl++++trelG+av++lGGGr+++dd+ lcl|FitnessBrowser__Smeli:SMc04122 301 RVLGSGEAMERFGLMVHRLGGPADFVDRPGAYLAKAPAILAVPAGRHGYLTSCKTRELGMAVIELGGGRIRPDDR 375 *************************************************************************** PP TIGR02643 376 ldlsvGltdllelGekvekeeplavvhaadeedaeeaakavkkalkiadeaPeeakvvler 436 +d++vGlt l++lG+kvek+ep+a+vhaad+++ae++ak+v+++++iade+P++++v++++ lcl|FitnessBrowser__Smeli:SMc04122 376 IDHRVGLTGLRPLGTKVEKGEPIAFVHAADQSQAEAIAKRVVTLYAIADEEPARRPVIVSK 436 **********************************************************987 PP Internal pipeline statistics summary: ------------------------------------- Query model(s): 1 (437 nodes) Target sequences: 1 (440 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: 10.01 // [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:
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