Align Aspartate kinase; Aspartokinase; EC 2.7.2.4 (characterized)
to candidate PfGW456L13_1981 Aspartokinase (EC 2.7.2.4)
Query= SwissProt::C3JXY0 (413 letters) >FitnessBrowser__pseudo13_GW456_L13:PfGW456L13_1981 Length = 413 Score = 745 bits (1924), Expect = 0.0 Identities = 390/413 (94%), Positives = 401/413 (97%) Query: 1 MALIVQKFGGTSVGSVERIEQVADKVKKFRDAGDDLVVVLSAMSGETNRLIDLAKAISGD 60 MALIVQKFGGTSVG+VERIEQVADKVKKFRDAGDDLVVVLSAMSGETNRLIDLAK ISGD Sbjct: 1 MALIVQKFGGTSVGTVERIEQVADKVKKFRDAGDDLVVVLSAMSGETNRLIDLAKQISGD 60 Query: 61 QQPLPRELDVIVSTGEQVTIALLAMALNKRGVPAVSYTGSQVRILTDSAHTKARILQIDD 120 QP+PRELDVIVSTGEQVTIALLAMAL KRGVPAVSYTG+QVRILTDSAH KARILQIDD Sbjct: 61 GQPVPRELDVIVSTGEQVTIALLAMALIKRGVPAVSYTGNQVRILTDSAHNKARILQIDD 120 Query: 121 QKIRTDLKAGRVVVVAGFQGVDEQGNITTLGRGGSDTTGVALAAALKADECQIYTDVDGV 180 QKIR DLKAGRVVVVAGFQGVDE GNITTLGRGGSDTTGVALAAALKADECQIYTDVDGV Sbjct: 121 QKIRGDLKAGRVVVVAGFQGVDEHGNITTLGRGGSDTTGVALAAALKADECQIYTDVDGV 180 Query: 181 YTTDPRVVSVAQRLDKITFEEMLEMASLGSKVLQIRAVEFAGKYNVPLRVLHSFKEGPGT 240 YTTDPRVVSVAQRLDKITFEEMLEMASLGSKVLQIRAVEFAGKYNVPLRVLHSFKEGPGT Sbjct: 181 YTTDPRVVSVAQRLDKITFEEMLEMASLGSKVLQIRAVEFAGKYNVPLRVLHSFKEGPGT 240 Query: 241 LITIDEEESMEQPIISGIAFNRDEAKLTIRGVPDTPGVAFKILGPISGANIEVDMIVQNV 300 LITIDEEE+MEQPIISGIAFNRDEAKLTIRGVPD PGVAFKILGPIS ANIEVDMIVQNV Sbjct: 241 LITIDEEETMEQPIISGIAFNRDEAKLTIRGVPDIPGVAFKILGPISAANIEVDMIVQNV 300 Query: 301 SHDNTTDFTFTVHRNEYDAAERILQNTAKEIGAREVVGDTKIAKVSIVGVGMRSHAGVAS 360 +HDNTTDFTFTVHRN+Y AA+ +L+ TA E+GAREVVGDTKIAKVSIVGVGMRSHAGVAS Sbjct: 301 AHDNTTDFTFTVHRNDYQAAQAVLEKTAGELGAREVVGDTKIAKVSIVGVGMRSHAGVAS 360 Query: 361 RMFEALAKESINIQMISTSEIKVSVVIEEKYLELAVRALHTAFELDAPARQGE 413 RMFE+LAKESINIQMISTSEIKVSVVIEEKYLELAVRALHTAFELDAPARQGE Sbjct: 361 RMFESLAKESINIQMISTSEIKVSVVIEEKYLELAVRALHTAFELDAPARQGE 413 Lambda K H 0.316 0.133 0.357 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: 698 Number of extensions: 23 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: 413 Length of database: 413 Length adjustment: 31 Effective length of query: 382 Effective length of database: 382 Effective search space: 145924 Effective search space used: 145924 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 (21.6 bits) S2: 50 (23.9 bits)
Align candidate PfGW456L13_1981 (Aspartokinase (EC 2.7.2.4))
to HMM TIGR00656 (aspartate kinase, monofunctional class (EC 2.7.2.4))
# 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.aa/TIGR00656.hmm # target sequence database: /tmp/gapView.26523.genome.faa # - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - Query: TIGR00656 [M=407] Accession: TIGR00656 Description: asp_kin_monofn: aspartate kinase, monofunctional class 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 ------- ------ ----- ------- ------ ----- ---- -- -------- ----------- 2.7e-133 430.8 13.4 3e-133 430.7 13.4 1.0 1 lcl|FitnessBrowser__pseudo13_GW456_L13:PfGW456L13_1981 Aspartokinase (EC 2.7.2.4) Domain annotation for each sequence (and alignments): >> lcl|FitnessBrowser__pseudo13_GW456_L13:PfGW456L13_1981 Aspartokinase (EC 2.7.2.4) # score bias c-Evalue i-Evalue hmmfrom hmm to alifrom ali to envfrom env to acc --- ------ ----- --------- --------- ------- ------- ------- ------- ------- ------- ---- 1 ! 430.7 13.4 3e-133 3e-133 1 406 [. 1 405 [. 1 406 [. 0.97 Alignments for each domain: == domain 1 score: 430.7 bits; conditional E-value: 3e-133 TIGR00656 1 veliVqKFGGtsvgsserikkaakivlkelkegkkvvVVvSAmskvtdelvelae 55 + liVqKFGGtsvg +eri+++a++v+k g++ vVV+SAms++t++l++la+ lcl|FitnessBrowser__pseudo13_GW456_L13:PfGW456L13_1981 1 MALIVQKFGGTSVGTVERIEQVADKVKKFRDAGDDLVVVLSAMSGETNRLIDLAK 55 579***************************************************5 PP TIGR00656 56 llklleaisdeisprerdelvsvGEllssallssalrelgvkaealdgkeagilT 110 + + ++ pre d +vs+GE++++all++al ++gv a++++g++ ilT lcl|FitnessBrowser__pseudo13_GW456_L13:PfGW456L13_1981 56 ----QISGDGQPVPRELDVIVSTGEQVTIALLAMALIKRGVPAVSYTGNQVRILT 106 ....345567899****************************************** PP TIGR00656 111 ddefgnAkikelateerLlelLeegiivvvaGFiGateeGeiTtLGRGGSDltAa 165 d+ +++A+i +++ +++ L+ g +vvvaGF+G +e+G+iTtLGRGGSD+t + lcl|FitnessBrowser__pseudo13_GW456_L13:PfGW456L13_1981 107 DSAHNKARILQIDD-QKIRGDLKAGRVVVVAGFQGVDEHGNITTLGRGGSDTTGV 160 *************9.**************************************** PP TIGR00656 166 llaaalkAdrveiyTDVeGvyttDPrvveeakkidkisyeEalelAtlGakvlhp 220 +laaalkAd+++iyTDV+GvyttDPrvv+ a+++dki++eE+le+A+lG kvl+ lcl|FitnessBrowser__pseudo13_GW456_L13:PfGW456L13_1981 161 ALAAALKADECQIYTDVDGVYTTDPRVVSVAQRLDKITFEEMLEMASLGSKVLQI 215 ******************************************************* PP TIGR00656 221 ralelaveakvpilvrsskekeegTlitn....kkensslvkaialeknvarltv 271 ra+e+a +++vp++v +s+++ gTlit ++e++ ++++ia++++ a+lt+ lcl|FitnessBrowser__pseudo13_GW456_L13:PfGW456L13_1981 216 RAVEFAGKYNVPLRVLHSFKEGPGTLITIdeeeTMEQP-IISGIAFNRDEAKLTI 269 ***************************98665556666.**************** PP TIGR00656 272 egegmlgkrgilaeifkaLaeeeinvdlisqtese...tsislvvdeedvdeakk 323 + g+ + +g++ +i + ++ ++i vd+i+q ++ t+ +++v+++d ++a++ lcl|FitnessBrowser__pseudo13_GW456_L13:PfGW456L13_1981 270 R--GVPDIPGVAFKILGPISAANIEVDMIVQNVAHdntTDFTFTVHRNDYQAAQA 322 *..9***************************99988889**************** PP TIGR00656 324 aLkeesgaaelesleveedlavvsivgaglveapGvaseifkaleekninilmis 378 +L+++ g+++ +++ + ++a+vsivg+g++++ Gvas++f+ l+++ ini mis lcl|FitnessBrowser__pseudo13_GW456_L13:PfGW456L13_1981 323 VLEKTAGELGAREVVGDTKIAKVSIVGVGMRSHAGVASRMFESLAKESINIQMIS 377 ******************************************************* PP TIGR00656 379 ssetkisvlvdekdaekavrklheklee 406 +se+k+sv+++ek++e avr+lh ++e+ lcl|FitnessBrowser__pseudo13_GW456_L13:PfGW456L13_1981 378 TSEIKVSVVIEEKYLELAVRALHTAFEL 405 *************************997 PP Internal pipeline statistics summary: ------------------------------------- Query model(s): 1 (407 nodes) Target sequences: 1 (413 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: 0.02u 0.01s 00:00:00.03 Elapsed: 00:00:00.01 # Mc/sec: 10.78 // [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