Align succinyl-diaminopimelate desuccinylase (EC 3.5.1.18) (characterized)
to candidate PfGW456L13_4721 N-succinyl-L,L-diaminopimelate desuccinylase (EC 3.5.1.18)
Query= BRENDA::Q9KQ52 (377 letters) >FitnessBrowser__pseudo13_GW456_L13:PfGW456L13_4721 Length = 383 Score = 448 bits (1153), Expect = e-130 Identities = 228/375 (60%), Positives = 272/375 (72%), Gaps = 2/375 (0%) Query: 4 SPVLALAKELISRQSVTPADAGCQDLMIERLKALGFEIESMVFEDTTNFWARRGTQS-PL 62 SP L LA +LI R SVTP DA CQ M++RL GF +E M ED NFWA G P+ Sbjct: 8 SPTLQLAIDLIRRPSVTPIDADCQKQMMQRLGDAGFTLEPMRIEDVDNFWATHGQDDGPV 67 Query: 63 FVFAGHTDVVPAGPLSQWHTPPFEPTVID-GFLHGRGAADMKGSLACMIVAVERFIAEHP 121 FAGHTDVVP GP++ W PF + + G L GRGAADMKGSLA M VA ERF+ ++P Sbjct: 68 LCFAGHTDVVPTGPVAAWQIEPFNALIDEHGMLCGRGAADMKGSLAAMTVASERFVTDYP 127 Query: 122 DHQGSIGFLITSDEEGPFINGTVRVVETLMARNELIDMCIVGEPSSTLAVGDVVKNGRRG 181 +H+G + FLITSDEEGP +GT VVE L AR E +D CIVGEPSST VGDVVKNGRRG Sbjct: 128 NHKGKVAFLITSDEEGPAHHGTKAVVERLAARKERLDWCIVGEPSSTTLVGDVVKNGRRG 187 Query: 182 SITGDLKVKGTQGHVAYPHLANNPVHKALPALAELAATQWDEGNAYFPPTSFQIPNLQAG 241 S+ L V+G QGHVAYPHLA NP+H A PALAELAA WD GN +FPPTSFQI N+ +G Sbjct: 188 SLGAKLTVRGVQGHVAYPHLAKNPIHLAAPALAELAAEHWDHGNDFFPPTSFQISNVNSG 247 Query: 242 TGASNVIPGEFDVQFNFRFSTELTDEEIKRRVHSVLDAHGLDYDVKWTLSGQPFLTDTGE 301 TGA+NVIPG+ FNFRFSTE T E +++RV +LD HGLD+ + W LSG PFLT+ G Sbjct: 248 TGATNVIPGDLVAVFNFRFSTESTVEGLQKRVADILDKHGLDWHIDWALSGLPFLTEPGA 307 Query: 302 LLAAVVAAVEEVNHQAPALLTTGGTSDGRFIAQMGAQVVELGPVNATIHKVNECVRIADL 361 LL AV A+++++ + T+GGTSDGRFIA MG QVVELGPVNATIH+VNE V ADL Sbjct: 308 LLDAVSASIKDITGRETKASTSGGTSDGRFIATMGTQVVELGPVNATIHQVNERVLAADL 367 Query: 362 EKLTDMYQKTLNHLL 376 + LT++Y +TL LL Sbjct: 368 DVLTEIYYQTLIKLL 382 Lambda K H 0.318 0.135 0.403 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: 515 Number of extensions: 26 Number of successful extensions: 3 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: 377 Length of database: 383 Length adjustment: 30 Effective length of query: 347 Effective length of database: 353 Effective search space: 122491 Effective search space used: 122491 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: 50 (23.9 bits)
Align candidate PfGW456L13_4721 (N-succinyl-L,L-diaminopimelate desuccinylase (EC 3.5.1.18))
to HMM TIGR01246 (dapE: succinyl-diaminopimelate desuccinylase (EC 3.5.1.18))
# 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/TIGR01246.hmm # target sequence database: /tmp/gapView.19171.genome.faa # - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - Query: TIGR01246 [M=370] Accession: TIGR01246 Description: dapE_proteo: succinyl-diaminopimelate desuccinylase 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 ------- ------ ----- ------- ------ ----- ---- -- -------- ----------- 1.9e-163 529.7 0.0 2.2e-163 529.5 0.0 1.0 1 lcl|FitnessBrowser__pseudo13_GW456_L13:PfGW456L13_4721 N-succinyl-L,L-diaminopimelate d Domain annotation for each sequence (and alignments): >> lcl|FitnessBrowser__pseudo13_GW456_L13:PfGW456L13_4721 N-succinyl-L,L-diaminopimelate desuccinylase (EC 3.5.1.18) # score bias c-Evalue i-Evalue hmmfrom hmm to alifrom ali to envfrom env to acc --- ------ ----- --------- --------- ------- ------- ------- ------- ------- ------- ---- 1 ! 529.5 0.0 2.2e-163 2.2e-163 2 370 .] 11 381 .. 10 381 .. 0.98 Alignments for each domain: == domain 1 score: 529.5 bits; conditional E-value: 2.2e-163 TIGR01246 2 lelakeLisrksvtPndagaqeliaerLkklgfeieilefedtknlwatrgt.ee 55 l+la++Li+r+svtP da++q+ +++rL gf+ e +++ed+ n+wat+g+ + lcl|FitnessBrowser__pseudo13_GW456_L13:PfGW456L13_4721 11 LQLAIDLIRRPSVTPIDADCQKQMMQRLGDAGFTLEPMRIEDVDNFWATHGQdDG 65 5899***********************************************9789 PP TIGR01246 56 pvlvfaGhtDvvPaGelekWssdpfepee.rdGklygrGaaDmkgslaafvvaae 109 pvl+faGhtDvvP+G++ +W+ +pf++ + ++G+l grGaaDmkgslaa+ va+e lcl|FitnessBrowser__pseudo13_GW456_L13:PfGW456L13_4721 66 PVLCFAGHTDVVPTGPVAAWQIEPFNALIdEHGMLCGRGAADMKGSLAAMTVASE 120 *************************9976256*********************** PP TIGR01246 110 rfvkknadhkGslsllitsDeegeaidGtkkvvetlkerdelidyavvgePssvk 164 rfv+++++hkG++++litsDeeg a +Gtk+vve l +r+e +d+++vgePss+ lcl|FitnessBrowser__pseudo13_GW456_L13:PfGW456L13_4721 121 RFVTDYPNHKGKVAFLITSDEEGPAHHGTKAVVERLAARKERLDWCIVGEPSSTT 175 ******************************************************* PP TIGR01246 165 klGDvikiGrrGsitgklkikGiqGhvaYPhkaenPvhkavpvlkeliaiklDeG 219 +GDv+k+GrrGs+ +kl+++G+qGhvaYPh+a+nP+h a+p+l+el+a+++D+G lcl|FitnessBrowser__pseudo13_GW456_L13:PfGW456L13_4721 176 LVGDVVKNGRRGSLGAKLTVRGVQGHVAYPHLAKNPIHLAAPALAELAAEHWDHG 230 ******************************************************* PP TIGR01246 220 neffppsslqianieagtgasnviPgelkvkfnlrfssevseeelkskvekildk 274 n+ffpp+s+qi+n+++gtga+nviPg+l + fn+rfs+e+++e l+++v++ildk lcl|FitnessBrowser__pseudo13_GW456_L13:PfGW456L13_4721 231 NDFFPPTSFQISNVNSGTGATNVIPGDLVAVFNFRFSTESTVEGLQKRVADILDK 285 ******************************************************* PP TIGR01246 275 hkldYelewklsgepfltkegklikkvaeaieevlkkkpelstsGGtsDarfiak 329 h+ld++++w lsg pflt+ g l+++v ++i+ ++++++++stsGGtsD+rfia+ lcl|FitnessBrowser__pseudo13_GW456_L13:PfGW456L13_4721 286 HGLDWHIDWALSGLPFLTEPGALLDAVSASIKDITGRETKASTSGGTSDGRFIAT 340 ******************************************************* PP TIGR01246 330 lgaevvelGlvndtihkvneavkiedleklsevyeklleel 370 +g++vvelG+vn+tih+vne+v +dl+ l+e+y+++l++l lcl|FitnessBrowser__pseudo13_GW456_L13:PfGW456L13_4721 341 MGTQVVELGPVNATIHQVNERVLAADLDVLTEIYYQTLIKL 381 ************************************99876 PP Internal pipeline statistics summary: ------------------------------------- Query model(s): 1 (370 nodes) Target sequences: 1 (383 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: 10.61 // [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