GapMind for catabolism of small carbon sources

 

Alignments for a candidate for rocD in Trichodesmium erythraeum IMS101

Align Ornithine aminotransferase; Ornithine--oxo-acid aminotransferase; EC 2.6.1.13 (characterized)
to candidate WP_011612286.1 TERY_RS13140 glutamate-1-semialdehyde 2,1-aminomutase

Query= SwissProt::Q6CWC1
         (437 letters)



>NCBI__GCF_000014265.1:WP_011612286.1
          Length = 432

 Score =  128 bits (322), Expect = 3e-34
 Identities = 96/336 (28%), Positives = 155/336 (46%), Gaps = 31/336 (9%)

Query: 30  PVVFSRASGAHVWDPEGKEYLDFLSAYSAVNQGHCHPHIIQALVDQASKLTLSSRAFSND 89
           P+VF R  GA++WD +G +Y+D++  +     GH HP ++  L +   K T    +F   
Sbjct: 40  PIVFDRVQGAYIWDVDGNQYIDYVGTWGPAICGHAHPEVLNGLKEVLEKGT----SFGAP 95

Query: 90  CFA--SFSKFVTEFF-GYESVLPMNTGAEAVESALKLARRWGYMVKKIQPNEAIILGARG 146
           C    + +K V +     E +  +N+G EA  + L+L R +    K I+          G
Sbjct: 96  CALENTLAKMVIDAVPSIEMIRFVNSGTEACMAVLRLMRAFTGRDKVIK--------FEG 147

Query: 147 NFHGRT-FGAISLSTDEEDSRMNFGPFLENVTAKIPGGSDDEFIRYGEIDDYKRAFESHG 205
            +HG      +   +      +   P +     K     +     Y +++  K+ FE + 
Sbjct: 148 CYHGHADMFLVKAGSGVATLGLPDSPGVPKHVTK-----NTLTAPYNDLETVKKLFEENP 202

Query: 206 DKICAVIVEPIQGEAGIVVPRADFLTDLQELCKKHQVLLICDEIQTG--IARTGKLLCYE 263
           D+I  VI+EP+ G +G +VP A FL  L+ + K++  LL+ DE+ TG  IA  G     +
Sbjct: 203 DQISGVILEPVVGNSGFIVPDAGFLEGLRMITKENGALLVFDEVMTGFRIAYGGA----Q 258

Query: 264 HSPNCKPDIILLGKAISGGVLPVSCVLSSREIMDCFTPGS---HGSTYGGNPLASRVAIA 320
              N  PD+  LGK I GG LPV      ++IM    P        T  GNPLA    I 
Sbjct: 259 EKFNVTPDLTTLGKIIGGG-LPVGAYGGRQDIMSMVAPAGPMYQAGTLSGNPLAMTAGIK 317

Query: 321 ALEVVQNENLVERSARLGKFLQDELVKLQHESNGVI 356
            LE+++     ++  ++ K L D L+ +  E+N  I
Sbjct: 318 TLELLKKPGTYDQLNKITKRLADGLLNIAKETNNDI 353


Lambda     K      H
   0.318    0.136    0.400 

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: 385
Number of extensions: 16
Number of successful extensions: 4
Number of sequences better than 1.0e-02: 1
Number of HSP's gapped: 2
Number of HSP's successfully gapped: 2
Length of query: 437
Length of database: 432
Length adjustment: 32
Effective length of query: 405
Effective length of database: 400
Effective search space:   162000
Effective search space used:   162000
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)

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

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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:

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