GapMind for catabolism of small carbon sources

 

Alignments for a candidate for malK_Bb in Desulfacinum infernum DSM 9756

Align ABC-type maltose transport, ATP binding protein (characterized, see rationale)
to candidate WP_073037051.1 BUB04_RS03685 ABC transporter ATP-binding protein

Query= uniprot:Q6MNM2
         (347 letters)



>NCBI__GCF_900129305.1:WP_073037051.1
          Length = 361

 Score =  188 bits (477), Expect = 2e-52
 Identities = 118/337 (35%), Positives = 187/337 (55%), Gaps = 34/337 (10%)

Query: 1   MAKIQFSNIKKSFG------SADVLKGIDLDIAPGEFLVLVGPSGCGKSTLLRTLAGLES 54
           MA+I    +  S+       S   LK ID     G    L+GPSGCGK+T+L  ++GL +
Sbjct: 1   MARITLQEVAHSYRRHPKDPSDYALKNIDTVWEDGGAYALLGPSGCGKTTMLNIISGLLT 60

Query: 55  ADSGTISIDGKKINDIEPQNRDIAMVFQSYALYPHMTVAENMGFGLKLKNLAAAEITKRV 114
              G +  D + +  + P+ R+IA VFQ   LY  M+V +N+ F L+ + L    + +RV
Sbjct: 61  PTRGRVLYDDRDVTRLPPEQRNIAQVFQFPVLYDTMSVFDNLAFPLRNRGLDPQTVRRRV 120

Query: 115 NEISELLQIKHLLDRKPKELSGGQRQRVALGRALSRQ-TPVILFDEPLSNLDAHLRSQMR 173
            E++E+L +   L +K   LS   +Q+++LGR L R+    ILFDEPL+ +D HL+  +R
Sbjct: 121 QEVAEVLDLTADLKKKAAGLSADAKQKISLGRGLVREDVAAILFDEPLTVIDPHLKWHLR 180

Query: 174 LEIKRLHHNSKSTMIYVTHDQMEATTLGDRIAVLKDGVIEQIGTPSEIYHRPKNTFIATF 233
            ++K +H   + T+IYVTHDQ+EA T  D++ V+ +G + Q+GTP+E++  P++ F+  F
Sbjct: 181 RKLKEIHERLRLTLIYVTHDQVEALTFADKVLVMYEGEVVQMGTPTELFEEPRHKFVGYF 240

Query: 234 IGSPEMNF----LEGAVL----EKIPWPE--ARKADQ-----ILGIRPDAFALNQGPLGT 278
           IGSP MNF    L+GA        +P  E  AR+A +      LGIRP    ++  P   
Sbjct: 241 IGSPGMNFIPCKLDGARAVFDGAAVPLDEETARRAREKEGPFELGIRPMYLEVHDSP--- 297

Query: 279 QEVALGDFQIDIS----ENLGGQQMLHGTLAGNNVRI 311
                GD ++ +     E+ G  ++L   LA N +++
Sbjct: 298 -----GDDRLPVKVLKVEDQGIFRILTVQLASNTLKV 329


Lambda     K      H
   0.318    0.136    0.383 

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: 271
Number of extensions: 8
Number of successful extensions: 2
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: 347
Length of database: 361
Length adjustment: 29
Effective length of query: 318
Effective length of database: 332
Effective search space:   105576
Effective search space used:   105576
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 (21.7 bits)
S2: 49 (23.5 bits)

This GapMind analysis is from Apr 09 2024. 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