Aligments for a candidate for prpE in Cupriavidus basilensis 4G11

GapMind for catabolism of small carbon sources

Aligments for a candidate for prpE in Cupriavidus basilensis 4G11

Align 4-hydroxybutyrate-CoA ligase (EC 6.2.1.40) (characterized)
to candidate RR42_RS27915 RR42_RS27915 acyl-CoA synthetase

Query= BRENDA::A4YDR9
         (549 letters)



>lcl|FitnessBrowser__Cup4G11:RR42_RS27915 RR42_RS27915 acyl-CoA
           synthetase
          Length = 545

 Score =  390 bits (1003), Expect = e-113
 Identities = 215/530 (40%), Positives = 306/530 (57%), Gaps = 14/530 (2%)

Query: 22  LTPLLFLERAGKYFKDKTAVVYRDSRYTYSTFYDNVMVQASALMRRGFSREDKLSFISRN 81
           LTP+ FL RA   + D+ A+V+   R  +   Y      AS L   G  + D ++ +  N
Sbjct: 19  LTPIDFLARAASVYGDRLAIVHGPVRQNWRDTYARARRLASGLASLGVGKGDTVAALLPN 78

Query: 82  RPEFLESFFGVPYAGGVLVPINFRLSPKEMAYIINHSDSKFVVVDEPYLNSLLEVKDQIK 141
            P  +E+ FGVP AG VL  +N RL    + +++ H +++ ++ D  + +   ++ ++I 
Sbjct: 79  TPAMVEAHFGVPMAGAVLNALNIRLDASNLIFMLRHGEARVLLADTEFADVARQIANEIP 138

Query: 142 -----AEIILLEDPDNPSASETARKEVRMTYRELVKGGSRDPLPIPAKEEYSMITLYYTS 196
                A +  L   D P+  ET  +      R L  G       +PA +E+  I L YTS
Sbjct: 139 GLKVVAVLDALGPQDAPAFGETDYE------RLLASGDPEFAWQMPA-DEWDAIALNYTS 191

Query: 197 GTTGLPKGVMHHHRGAFLNAMAEVLEHQMDLNSVYLWTLPMFHAASWGFSWATVAVGATN 256
           GTTG PKGV++HHRGA +NA++ +LE  +  ++VYLWTLPMFH   W F W   A    N
Sbjct: 192 GTTGDPKGVVYHHRGAAINAISNILEWDLPKHAVYLWTLPMFHCNGWCFPWTIAARAGVN 251

Query: 257 VCLDKVDYPLIYRLVEKERVTHMCAAPTVYVNLADYMKRNNLKFSNRVHMLVAGAAPAPA 316
           VCL K +  L++ L+  E VTH CAAP V+  L +            V  +VAGA P  A
Sbjct: 252 VCLRKFEPKLVFDLMRDEGVTHYCAAPIVHTALVNAPLAWRDGVRGPVRGMVAGAPPPAA 311

Query: 317 TLKAMQEIGGYMCHVYGLTETYGPHSICEWRREWDSLPLEEQAKLKARQGIPY-VSFEMD 375
            L  M+ +G  + HVYGLTETYGP ++C  + +W SL  E++A  KARQG+ Y +  E+ 
Sbjct: 312 VLAQMEAMGFALTHVYGLTETYGPAAVCAEQDDWASLSQEDRATKKARQGVRYHLQTEVA 371

Query: 376 VFDANG-KPVPWDGKTIGEVVMRGHNVALGYYKNPEKTAESFRDGWFHSGDAAVVHPDGY 434
           V D +  +PV  DG+ IGE++ RG+    GY KN + T E+F  GWFH+GD  V  PDGY
Sbjct: 372 VLDPDTMQPVASDGEEIGEIMFRGNICMKGYLKNEKATREAFAGGWFHTGDLGVCTPDGY 431

Query: 435 IEIVDRFKDLINTGGEKVSSILVEKTLMEIPGVKAVAVYGTPDEKWGEVVTARIELQEGV 494
           ++I DR KD+I +GGE +SS+ VE  +   P V AVAV   PD KWGE   A +EL++G 
Sbjct: 432 VKIKDRSKDIIISGGENISSVEVEDAIYRHPAVLAVAVVAQPDVKWGETPCAFVELKDGA 491

Query: 495 KLTEEEVIKFCKERLAHFECPKIVEFGPIPMTATGKMQKYVLRNEAKAKA 544
             T +E+I  C+  LA F+ PK V FGP+P T+TGK+QK+ LR + K+ A
Sbjct: 492 SATADELIAHCRTLLAGFKVPKAVYFGPLPKTSTGKIQKFELRKKVKSDA 541


Lambda     K      H
   0.319    0.136    0.411 

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: 764
Number of extensions: 31
Number of successful extensions: 4
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: 549
Length of database: 545
Length adjustment: 36
Effective length of query: 513
Effective length of database: 509
Effective search space:   261117
Effective search space used:   261117
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: 52 (24.6 bits)

This GapMind analysis is from Sep 17 2021. The underlying query database was built on Sep 17 2021.

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Protein sequences (fasta format)
Organisms (tab-delimited)
SQLite3 databases

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About GapMind

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:

ublast finds a hit to a characterized protein at above 40% identity and 80% coverage, and bits >= other bits+10.
- (Hits to curated proteins without experimental data as to their function are never considered high confidence.)
HMMer finds a hit with 80% coverage of the model, and either other identity < 40 or other coverage < 0.75.

where "other" refers to the best ublast hit to a sequence that is not annotated as performing this step (and is not "ignored").

Otherwise, a candidate is "medium confidence" if either:

ublast finds a hit at above 40% identity and 70% coverage (ignoring otherBits).
ublast finds a hit at above 30% identity and 80% coverage, and bits >= other bits.
HMMer finds a hit (regardless of coverage or other bits).

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:

our ignorance of proteins' functions,
omissions in the gene models,
frame-shift errors in the genome sequence, or
the organism lacks the pathway.

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

GapMind for catabolism of small carbon sources