GapMind for catabolism of small carbon sources

 

Alignments for a candidate for xdh in Marinobacter adhaerens HP15

Align D-xylose 1-dehydrogenase (NADP+) (EC 1.1.1.179) (characterized)
to candidate GFF1627 HP15_1586 oxidoreductase N-terminal domain-containing protein

Query= BRENDA::D4GP30
         (325 letters)



>FitnessBrowser__Marino:GFF1627
          Length = 348

 Score =  138 bits (348), Expect = 2e-37
 Identities = 108/344 (31%), Positives = 157/344 (45%), Gaps = 30/344 (8%)

Query: 3   FGILGTAGIGVKSVIPAVQASEHEAAAIASRDEARASAVADELGIPTAYGSYEALLADDS 62
           +GI+GTA I  K V     A   +  A+ASR   RA A ADE  +P A GSY+ LLAD+S
Sbjct: 8   WGIIGTAEIATKVVAGMHDAENADVVAVASRSLDRAQAWADEHDVPQALGSYDELLADES 67

Query: 63  LDAVYIPLPNGLHADWVRAAADRGLHVLCEKPLTASADETAAVFDYCEDAGVTLMEAFMY 122
           +D VYIP+P  L  +W++ AA  G HV  EKPL   AD      D C++ GV  M+  M+
Sbjct: 68  IDGVYIPVPTALRNEWIKKAARAGKHVYAEKPL---ADGIEEAIDVCKENGVQFMDGTMW 124

Query: 123 RFHPLTERAAELVAS-ELGAVVSVTSNFSFRLP--------DGADDIRIDPDLAGGSVMD 173
                T+   + +A+ ++G V  VTS F+F+ P        +G  D   +P    G   D
Sbjct: 125 LHSNRTQDIEQRIANGDIGDVRRVTSAFTFKAPNKEWYEGGNGRTDKSREP---MGCFGD 181

Query: 174 VGCYAVSAARLFLG--TPDRVYATTTDTRDCGVDTRMSGVLEYDSGATA----------- 220
            G Y +SA     G   P+RV  T              G L +  G  A           
Sbjct: 182 QGWYPISATMWSFGYELPERVQMTFVSKNSIDTIVACGGTLWFSDGRMATFDAGCELAHR 241

Query: 221 -RVESSFDTPETQYYRVQTTDGRLEANPAFNVDPTAAAELTYA-TDGRVVTETFDPTDSY 278
            +VE+  D    +   +    GR     A+    T ++       DG+   +  +P D  
Sbjct: 242 SQVETVGDAGLIRIDDLVGGQGRTGNFAAYGERFTGSSHYVLGDADGKDTEQEVEPCDHV 301

Query: 279 RREVEAFARAVETGETPRVDREESVSVMRTIDAIYESAETGAAV 322
            + VE F+  + TGE      + S++  R + A++ESAE+  AV
Sbjct: 302 VKLVEKFSNIILTGEIDDQWPKRSLACHRVMSALFESAESNGAV 345


Lambda     K      H
   0.316    0.131    0.371 

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: 281
Number of extensions: 19
Number of successful extensions: 3
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: 325
Length of database: 348
Length adjustment: 28
Effective length of query: 297
Effective length of database: 320
Effective search space:    95040
Effective search space used:    95040
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.

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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