GapMind for catabolism of small carbon sources

 

Alignments for a candidate for sdaB in Planktomarina temperata RCA23

Align Threonine dehydratase 2 biosynthetic, chloroplastic; SlTD2; Threonine deaminase 2; EC 4.3.1.17; EC 4.3.1.19 (characterized)
to candidate WP_044051092.1 RCA23_RS15620 threonine ammonia-lyase IlvA

Query= SwissProt::P25306
         (595 letters)



>NCBI__GCF_000738435.1:WP_044051092.1
          Length = 411

 Score =  201 bits (512), Expect = 4e-56
 Identities = 135/393 (34%), Positives = 207/393 (52%), Gaps = 13/393 (3%)

Query: 113 SPLELAEKLSDRLGVNFYIKREDKQRVFSFKLRGAYNMMSNLSREELDKGV-ITASAGNH 171
           +PL+  + LS+    + ++KRED   V S+KLRGA+N M     ++ DK V + ASAGNH
Sbjct: 22  TPLQRNDHLSNVYDADIWLKREDLSPVRSYKLRGAFNAMG----KQADKDVFVCASAGNH 77

Query: 172 AQGVALAGQRLNCVAKIVMPTTTPQIKIDAVRALGG---DVVLYGKTFDEAQTHALELSE 228
           AQGVA   + L     I MP TTP+ KI   R  GG    V L G  FD+    +     
Sbjct: 78  AQGVAYVCRHLQKKGVIFMPVTTPEQKIRKTRLFGGAWVQVQLVGDYFDDTLRASQAYCA 137

Query: 229 KDGLKYIPPFDDPGVIKGQGTIGTEINRQLKDIHAVFI-PVGGGGLIAGVATFFKQIAPN 287
           + G  ++ PFDDP VI+GQ T+  E+  QL     VF+ PVGGGGL +       + AP 
Sbjct: 138 EVGGHFLSPFDDPDVIEGQATVTYEMLEQLGRSPDVFVVPVGGGGLSSSARRLLSERAPE 197

Query: 288 TKIIGVEPYGAASMTLSLHEGHRVKLSNVDTFADGVAVALVGEYTFAKCQEL-IDGMVLV 346
           T+I  VEP G  S+  ++  G  + L  VDTF DG AVA +G  TFA  + +  D ++ +
Sbjct: 198 TEIFYVEPSGGKSLAAAVQAGAPIALEQVDTFVDGAAVAKMGVNTFAALKGIDADHVLDI 257

Query: 347 ANDGISAAIKDVYDEGRNILETSGAVAIAGAAAYCEFYKIKNENIVAIASGANMDFSKLH 406
             D I   I D+ +    +LE +GA+A+       +  KIK + +V ++SG N DF +L 
Sbjct: 258 PEDRICTTILDMLNTEGIVLEPAGALALDALKDLKD--KIKGKTVVCVSSGGNFDFERLP 315

Query: 407 KVTELAGLGSGKEALLATFMVEQQGSFKTFVGLVG-SLNFTELTYRFTSERKNALILYRV 465
           +V E A   +G +      + ++ G+ K F+GL+G   +     Y   S R    +L  +
Sbjct: 316 EVKERAQRYAGVKKYFILRLPQRPGALKDFLGLLGPDDDIARFEYLKKSARNFGTVLLGI 375

Query: 466 NVDKESDLEKMIEDMKSSNMTTLNLSHNELVVD 498
              K  +   + E ++++ M+  +++ +E +VD
Sbjct: 376 ETSKPENFALLSERLEAAGMSIRDITGDEAMVD 408


Lambda     K      H
   0.317    0.135    0.382 

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: 550
Number of extensions: 31
Number of successful extensions: 5
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: 595
Length of database: 411
Length adjustment: 34
Effective length of query: 561
Effective length of database: 377
Effective search space:   211497
Effective search space used:   211497
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 (21.7 bits)
S2: 52 (24.6 bits)

This GapMind analysis is from Sep 24 2021. The underlying query database was built on Sep 17 2021.

Links

Downloads

Related tools

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:

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:

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