GapMind for catabolism of small carbon sources

 

Alignments for a candidate for DVU3033 in Marinobacter adhaerens HP15

Align Iron-sulfur cluster-binding protein (characterized, see rationale)
to candidate GFF4149 HP15_4089 iron-sulfur cluster binding protein

Query= uniprot:Q726S3
         (717 letters)



>FitnessBrowser__Marino:GFF4149
          Length = 483

 Score =  295 bits (756), Expect = 3e-84
 Identities = 155/380 (40%), Positives = 225/380 (59%), Gaps = 2/380 (0%)

Query: 9   EYRKELQESLDNEFLRNAMDKFAVAYRASRANAFKDIDEKAIIAEVADA-KDHAAKNMDT 67
           ++R   +E+L +  LRN       +    RANAF D DE+  + E+ +  K  A   +  
Sbjct: 13  DFRGRAEEALADGQLRNNFRVAMDSLMTKRANAFPDADEREGLRELGNRIKAGALSRLPD 72

Query: 68  LYAQFKAEAEKRGVKVHLARTAAEANEIIARIARDNNCKKAIKSKSMTAEETHLNHRLEE 127
           L  Q + +  + GVKVH A T  EAN ++  I       + +K KSM +EE  +N  L E
Sbjct: 73  LLEQLEQKLTENGVKVHWAETVEEANSLVHGIIEARKGSQVVKGKSMVSEEMEMNDYLAE 132

Query: 128 DNVEVIETDLGEWIIQMRHEGPSHMVMPAIHLSRYQVADLFSEVTKQKQEVDIQRLVKVA 187
             VE +E+D+GE+I+Q+ +E PSH++MPAIH +  QV+ LF +   + +  D+ +L+++ 
Sbjct: 133 RGVECLESDMGEYIVQLDNEKPSHIIMPAIHKNARQVSKLFHDKLGEPETEDVNQLIQIG 192

Query: 188 RRELRTHFATADMGISGANFAVAETGTIGLVTNEGNARLVTTLPRVHVALAGLDKLVPTL 247
           RR LR  F  AD+G+SG NFA+AETGT+ LV NEGN R+ TT P VH+A+ G++K+VP L
Sbjct: 193 RRTLRRKFMEADVGVSGVNFAIAETGTLLLVENEGNGRMSTTAPPVHIAVTGIEKVVPNL 252

Query: 248 HDALRSLKVLPRNATGQAITSYVTWIGGANECEACVDGRKEMHIVFLDNGRRALAEDPLF 307
            D +  + +L R+A GQ IT+YV  I G  + +  +DG +E+H+V LDNGR     D   
Sbjct: 253 RDVVPLVSLLTRSALGQPITTYVNLISGPRKPDE-LDGPEEVHLVLLDNGRTGAFADAQM 311

Query: 308 SQVLRCVRCGACANVCPVYRLVGGHKMGHIYIGAIGLILTYFFHGRDKARNLVQNCINCE 367
            Q L C+RCGAC N CPVY  VGGH  G +Y G IG I+T    G DK  +       C 
Sbjct: 312 RQTLNCIRCGACMNHCPVYTRVGGHTYGEVYPGPIGKIITPHMAGLDKVPDHPSASSLCG 371

Query: 368 SCKHICAGGIDLPRLIKEIR 387
           +C  +C   I +P L++ +R
Sbjct: 372 ACGEVCPVKIPIPELLQRLR 391


Lambda     K      H
   0.321    0.135    0.402 

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: 778
Number of extensions: 39
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: 717
Length of database: 483
Length adjustment: 37
Effective length of query: 680
Effective length of database: 446
Effective search space:   303280
Effective search space used:   303280
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 (21.9 bits)
S2: 53 (25.0 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