GapMind for catabolism of small carbon sources

 

Alignments for a candidate for dhaD in Salinicoccus carnicancri Crm

Align Glycerol dehydrogenase; GDH; GLDH; GlyDH; EC 1.1.1.6 (characterized)
to candidate WP_017549469.1 C792_RS0110820 glycerol dehydrogenase

Query= SwissProt::P32816
         (370 letters)



>NCBI__GCF_000330705.1:WP_017549469.1
          Length = 365

 Score =  385 bits (989), Expect = e-111
 Identities = 192/364 (52%), Positives = 259/364 (71%), Gaps = 1/364 (0%)

Query: 3   AERVFISPAKYVQGKNVITKIANYLEGIGNKTVVIADEIVWKIAGHTIVNELKKGNIAAE 62
           A+ VF SP KY+QG+ V+  +      +  K +VI+DE+VW I    I        I  +
Sbjct: 2   AKYVFQSPGKYIQGQGVLETLGEETGKLAAKPLVISDEMVWSITEQKITESFNNAGIDFK 61

Query: 63  EVVFSGEASRNEVERIANIARKAEAAIVIGVGGGKTLDTAKAVADELDAYIVIVPTAAST 122
              F GEAS  E+ R+ ++A   +A  VIGVGGGKTLDT+KA+AD L + ++IVPT AST
Sbjct: 62  YEEFEGEASEAEISRLTDVAENNDADAVIGVGGGKTLDTSKAIADNLGSPVIIVPTTAST 121

Query: 123 DAPTSALSVIYSDDGVFESYRFYKKNPDLVLVDTKIIANAPPRLLASGIADALATWVEAR 182
           DAP+S+LSVIYSD+G F  YRFY KNP L+++D+ ++ NAP  L ASG++DA+AT VEAR
Sbjct: 122 DAPSSSLSVIYSDEGAFTGYRFYDKNPSLIIIDSSVVVNAPAGLFASGMSDAMATLVEAR 181

Query: 183 SVIKSGGKTMAGGIPTIAAEAIAEKCEQTLFKYGKLAYESVKAKVVTPALEAVVEANTLL 242
           +  KS G  M GG PT+AA AIAEKCE+T+FK+G  AYE+    +VTP ++AV+EANTLL
Sbjct: 182 AAQKSNGDNMVGGQPTLAAAAIAEKCEETIFKHGHAAYEAASNGIVTPQVDAVIEANTLL 241

Query: 243 SGLGFESGGLAAAHAIHNGFTALEGEIHHLTHGEKVAFGTLVQLALEEHSQQEIERYIEL 302
           SGLGFE+GGLAAAHAIHNGFT+L G+IHHL+HGEKVA+GTLVQL LE    + + RYIE 
Sbjct: 242 SGLGFENGGLAAAHAIHNGFTSLSGDIHHLSHGEKVAYGTLVQLVLENSPDETLNRYIEF 301

Query: 303 YLSLDLPVTLEDIKLKDASREDILKVAKAATAEGETIHN-AFNVTADDVADAIFAADQYA 361
           Y ++ +P TL+++ L+D S ED++KV + AT   +T  N +  VT +++A+AI A    +
Sbjct: 302 YKNIGMPTTLKEMHLEDTSFEDLVKVGELATDPEDTFANLSDRVTPEEIANAILAVSTIS 361

Query: 362 KAYK 365
           +A K
Sbjct: 362 EAGK 365


Lambda     K      H
   0.314    0.131    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: 308
Number of extensions: 12
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: 370
Length of database: 365
Length adjustment: 30
Effective length of query: 340
Effective length of database: 335
Effective search space:   113900
Effective search space used:   113900
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: 42 (22.0 bits)
S2: 49 (23.5 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