GapMind for catabolism of small carbon sources

 

Alignments for a candidate for uxuB in Herbaspirillum seropedicae SmR1

Align D-mannonate oxidoreductase; EC 1.1.1.57; Fructuronate reductase (uncharacterized)
to candidate HSERO_RS02215 HSERO_RS02215 D-arabinitol 4-dehydrogenase

Query= curated2:P39160
         (486 letters)



>FitnessBrowser__HerbieS:HSERO_RS02215
          Length = 477

 Score =  194 bits (494), Expect = 4e-54
 Identities = 130/364 (35%), Positives = 192/364 (52%), Gaps = 16/364 (4%)

Query: 26  VHLGCGAFHRAHQALYTHHLLES-TDSDWGICEVNLMPGNDRVLIENLKKQQLLYT---V 81
           +H+G G+FHRAHQA+Y + L ES  D  W +   N+   +   L+E L +QQ  YT   V
Sbjct: 19  LHIGAGSFHRAHQAVYLNALRESGADRRWQLALANIR-ADMSPLLEALARQQGQYTLETV 77

Query: 82  AEKGAESTELKIIGSMKEALHPEIDGCEGILNAMARPQTAIVSLTVTEKGYCADAASGQL 141
             +G  S +   I S+   L P       ++ A A  +T I+S TVTE GY  D    QL
Sbjct: 78  TPQGQRSYQR--IASIGRIL-PWDAQLTQLIAAGAEERTRIISFTVTEGGYYLDHQH-QL 133

Query: 142 DLNNPLIKHDL----ENPTAPKSAIGYIVEALRLRREKGLKA-FTVMSCDNVRENGHVAK 196
           D +N  +  DL    +   AP++  G I   L  R +   +A  T+++CDN+R NG   +
Sbjct: 134 DTSNADLAEDLRCALDGSGAPRTIYGAIAAILHARSQAHPQAALTLLNCDNLRHNGERFR 193

Query: 197 VAVLGLAQAR-DPQLAAWIEENVTFPCTMVDRIVPAATPETLQEIADQLGVYDPCAIACE 255
             +      R +  L +W++ N T P  MVDRI P  T    Q + +  G+ DPCA+  E
Sbjct: 194 DGLRQFLTLRGETALVSWMQANTTSPNAMVDRITPRPTAAVAQRVKEATGIDDPCALMGE 253

Query: 256 PFRQWVIEDNFVNGRPDWDKVGAQFVADVVPFEMMKLRMLNGSHSFLAYLGYLGGYETIA 315
            F QWVIED+F  GRP  ++ G + V  V+P+E  K+R+LN SHS +A+ G L G + I 
Sbjct: 254 SFIQWVIEDDFKAGRPRLEEAGVEMVQSVLPYEEAKIRILNASHSCIAWAGTLAGLQYIH 313

Query: 316 DTVTNPAYRKAAFALMMQEQAPTLSMPEGTDLNAYATLLIERFSNPSLRHRTWQIAMDGS 375
           +       R+ A+  + Q+    L+ P   DL AY    + RFSNP+++    ++A DG 
Sbjct: 314 EGTLRDDIRQMAYDYVTQDVIACLT-PSPIDLAAYRDTTLARFSNPAIQDTNQRVAADGY 372

Query: 376 QKLP 379
            K+P
Sbjct: 373 SKIP 376


Lambda     K      H
   0.320    0.135    0.408 

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: 562
Number of extensions: 28
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: 486
Length of database: 477
Length adjustment: 34
Effective length of query: 452
Effective length of database: 443
Effective search space:   200236
Effective search space used:   200236
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 (21.8 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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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