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 GFF2943 HP15_2887 iron-sulfur cluster binding protein

Query= uniprot:Q726S3
         (717 letters)



>FitnessBrowser__Marino:GFF2943
          Length = 479

 Score =  287 bits (734), Expect = 1e-81
 Identities = 152/381 (39%), Positives = 221/381 (58%), Gaps = 1/381 (0%)

Query: 7   LKEYRKELQESLDNEFLRNAMDKFAVAYRASRANAFKDIDEKAIIAEVADAKDHAAKNMD 66
           +KE+    Q ++ +  +R           + R  AF+  D + +    A+ +  A  N+ 
Sbjct: 14  VKEFHPRAQAAIHDPKIRKNFRSAMDGLMSKRKTAFEGWDLETLRDLGANVRLRALANLP 73

Query: 67  TLYAQFKAEAEKRGVKVHLARTAAEANEIIARIARDNNCKKAIKSKSMTAEETHLNHRLE 126
            L  Q + +  + G+KVH A    EA  I+  I +  + K  IK KSM +EE  LNH LE
Sbjct: 74  DLLEQLEKKLIENGIKVHWAVDGDEACRIVRDICKARDAKTVIKGKSMVSEEMELNHYLE 133

Query: 127 EDNVEVIETDLGEWIIQMRHEGPSHMVMPAIHLSRYQVADLFSEVTKQKQEVDIQRLVKV 186
           E  +E +E+DLGE+I+Q+  E PSH++MPAIH +  +++ L  E T      D++ L   
Sbjct: 134 EQGIEALESDLGEYIVQLADETPSHIIMPAIHKNTGEISQLLHEKTGTDLSNDVEYLTAS 193

Query: 187 ARRELRTHFATADMGISGANFAVAETGTIGLVTNEGNARLVTTLPRVHVALAGLDKLVPT 246
           AR +LR  F  AD+G+SG NFAVAETGT+ LV NEGN R+ TT+P+ H+A+ G++K+VP+
Sbjct: 194 ARLQLREKFMNADVGVSGVNFAVAETGTLCLVENEGNGRMTTTVPKCHIAVTGIEKVVPS 253

Query: 247 LHDALRSLKVLPRNATGQAITSYVTWIGGANECEACVDGRKEMHIVFLDNGRRALAEDPL 306
           + D    L +L R+ATGQ IT+Y   I G  + E  +DG +E+H+V +DNGR ++ +D  
Sbjct: 254 MEDVSALLALLTRSATGQHITTYFNMISGPRKAEE-LDGPEEVHLVLVDNGRSSIYQDDE 312

Query: 307 FSQVLRCVRCGACANVCPVYRLVGGHKMGHIYIGAIGLILTYFFHGRDKARNLVQNCINC 366
               LRC+RCGAC N CPVY  VGGH  G  Y G IG IL     G D+ R+L      C
Sbjct: 313 LLDTLRCIRCGACMNHCPVYTRVGGHAYGTTYPGPIGKILMPHLIGLDEGRHLPSASSLC 372

Query: 367 ESCKHICAGGIDLPRLIKEIR 387
            +C  +C   I +P L+  +R
Sbjct: 373 GACGEVCPVKIPIPDLLVRLR 393


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: 766
Number of extensions: 30
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: 717
Length of database: 479
Length adjustment: 37
Effective length of query: 680
Effective length of database: 442
Effective search space:   300560
Effective search space used:   300560
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