GapMind for catabolism of small carbon sources

 

Alignments for a candidate for xyrA in Marinobacter adhaerens HP15

Align D-xylose reductase (EC 1.1.1.307) (characterized)
to candidate GFF2883 HP15_2827 oxidoreductase, aldo/keto reductase family

Query= BRENDA::F2YCN5
         (340 letters)



>FitnessBrowser__Marino:GFF2883
          Length = 329

 Score =  386 bits (991), Expect = e-112
 Identities = 190/329 (57%), Positives = 240/329 (72%), Gaps = 3/329 (0%)

Query: 12  DKISIKGIDKSATRVALGTWAIGGWMWGGTDDDASIKTIHRAIDLGINIIDTAPAYGRGH 71
           DK +    D   T V LGTWAIGGWMWGGTD+  SI TIHRAID GI ++DTAP YG G 
Sbjct: 2   DKRTFGNTDIQVTPVGLGTWAIGGWMWGGTDEAQSIDTIHRAIDKGIGLVDTAPVYGFGR 61

Query: 72  AEEVVGKAIK-GQRDNLIIATKVGLDWTLTPDQSMRRNSSASRIKKEIEDSLRRLGTDYI 130
           +EE+VGKA+  G+RD + +ATKV L+W    D+ + R++SASRI++E+EDSL+RL TD I
Sbjct: 62  SEEIVGKALSDGRRDQVALATKVALNWNDDHDK-VWRDASASRIEREVEDSLKRLQTDRI 120

Query: 131 DLYQVHWPDPLVPIEETATILEALRKEGKIRSIGVSNYSVQQMDEFKKYAELAVSQSPYN 190
           D+YQVHWPDP  P+EETA  LE L + GKIR+IGVSN++  QMDE +K   L   Q PYN
Sbjct: 121 DIYQVHWPDPKTPMEETARALEKLYQAGKIRAIGVSNFTPSQMDELQKSVPLHSLQPPYN 180

Query: 191 LFEREIDKDILPYAKKNDLVVLGYGALCRGLLSGRMTADRAFTGDDLRKTDPKFQKPRFE 250
           LFEREI++DILPY ++N +  + YG LCRG L+G+M  D  FTGDDLRK DPKFQ  R+ 
Sbjct: 181 LFEREIEQDILPYCRENGIATITYGGLCRGFLTGKMREDTQFTGDDLRKNDPKFQGDRYR 240

Query: 251 HYLAAVEELKKLAKEHYNKSVLALAIRWMLEQ-GPTLALWGACKPEQIDGIDEVFGWQIS 309
            YL AV EL   A+E Y KSVLALA+RW+++Q G T ALWGA +PEQ+D +DE+ GW + 
Sbjct: 241 QYLNAVAELDAFARERYQKSVLALALRWLVDQPGVTTALWGARRPEQLDPVDEIDGWSLD 300

Query: 310 DEDLKQIDAILAKNIPNPIGAEFMAPPPR 338
              + +ID IL + I +P+G EFMAPP R
Sbjct: 301 KNAMAEIDGILDRCITDPVGPEFMAPPTR 329


Lambda     K      H
   0.317    0.136    0.407 

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: 412
Number of extensions: 13
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: 340
Length of database: 329
Length adjustment: 28
Effective length of query: 312
Effective length of database: 301
Effective search space:    93912
Effective search space used:    93912
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: 49 (23.5 bits)

This GapMind analysis is from Sep 17 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