GapMind for catabolism of small carbon sources

 

Alignments for a candidate for dctP in Photobacterium gaetbulicola Gung47

Align TRAP dicarboxylate transporter DctP subunit; Flags: Precursor (characterized, see rationale)
to candidate WP_044620695.1 H744_RS01505 TRAP transporter substrate-binding protein

Query= uniprot:Q2IUT5
         (332 letters)



>NCBI__GCF_000940995.1:WP_044620695.1
          Length = 351

 Score =  171 bits (433), Expect = 2e-47
 Identities = 101/304 (33%), Positives = 165/304 (54%), Gaps = 5/304 (1%)

Query: 20  AAAQQPIVVKFSHVVADNTPKGQAAIKFKELAEKYTNGKVKVEVYPNSQLFGDAKEMEAV 79
           A   Q   ++FS       P    A KFKEL EK T+  + V++YP++QL  D   +E +
Sbjct: 37  ACESQIKTLRFSMSSNTQHPIYDGASKFKELVEKTTD--LTVDIYPSAQLGDDRAAIEML 94

Query: 80  ALGDVQFIAPSLSKFDKFTKQIQVFDLPFLFNDIAAVDRFQAGKQGQALLRSMESKNFLG 139
            LG +    PS +    F  +  VFDLPF+  + A  D+         +L  ++S+  +G
Sbjct: 95  QLGTLDVSIPSTAPLANFYPEYNVFDLPFMIPNEAVADKVLRSDFAGDMLEMLQSRRLIG 154

Query: 140 LAYWHNGMKQIS-ANRPLLKPEDAKGLKFRIQASDILAAQFQGLNATPQKLAFSEVYQAL 198
           L +W NG + ++ + R +   +D KGLK R   S +    ++ L ATP  +AF+E++ AL
Sbjct: 155 LDFWENGFRHLTNSRRTVTSVDDVKGLKVRTMESPLHLDAWKALGATPTPMAFNELFTAL 214

Query: 199 QVGTVDGQENTWSNIFSQKFYEVQKDITESDHGVIDYMVVVNAKWWNGLSKDLQDAMKKA 258
           Q GTVDGQEN + NI     YEVQK +T++ H     +++ +   WN LS   Q A+++A
Sbjct: 215 QQGTVDGQENPYPNIALNNLYEVQKQMTDTGHVYTPLVLIFSEASWNKLSAHDQAAVRQA 274

Query: 259 MDEATKVNNDVAGKLNDEAKQKIASSGASKIHQLTPEQRKQWVEAMKPVWAKFESAIGKD 318
             EA     +V  ++N+++   I ++   ++ +LTPE R ++ +A + V  K+   IG D
Sbjct: 275 AIEAGDYQREVNRRVNNDSLATIKAN--MQVTELTPEARSEFRKATESVVDKYRDVIGGD 332

Query: 319 LIDA 322
           +ID+
Sbjct: 333 IIDS 336


Lambda     K      H
   0.316    0.129    0.367 

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: 285
Number of extensions: 20
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: 332
Length of database: 351
Length adjustment: 29
Effective length of query: 303
Effective length of database: 322
Effective search space:    97566
Effective search space used:    97566
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 24 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