GapMind for catabolism of small carbon sources

 

Alignments for a candidate for mtlK in Desulfovibrio vulgaris Hildenborough

Align ABC transporter for D-Mannitol, D-Mannose, and D-Mannose, ATPase component (characterized)
to candidate 207786 DVU2299 glycine/betaine/L-proline ABC transporter, ATP binding protein

Query= reanno::pseudo13_GW456_L13:PfGW456L13_3039
         (367 letters)



>MicrobesOnline__882:207786
          Length = 397

 Score =  168 bits (425), Expect = 3e-46
 Identities = 109/319 (34%), Positives = 172/319 (53%), Gaps = 24/319 (7%)

Query: 21  GID---LEVNDKEFVVFVGPSGCGKSTLLRLIAGLEEVSGGTIELDGRDITEVSP----- 72
           G+D    +V + E VV +G SG GKSTL+R +  L E + GT+ +DGRD+T +       
Sbjct: 42  GVDRASFDVEEGEIVVVMGLSGSGKSTLVRCLNRLIEPTAGTVTVDGRDVTSMPVDELRR 101

Query: 73  -AKRDLAMVFQTYALYPHMSVRKNMSFALDLAGVAKAEVEKKVSEAARILELGPMLERKP 131
             +R   MVFQ +AL+PH +V +N +F L+  GV +AE E++   +   + L      +P
Sbjct: 102 LRQRSFGMVFQNFALFPHRTVLQNAAFGLEAMGVPRAERERQAMVSLERVGLAEWAASRP 161

Query: 132 KQLSGGQRQRVAIGRAIVRNPKIFLFDEPLSNLDAALRVQMRLELLRLHKELQATMIYVT 191
            QLSGG +QRV + RA+  +P I L DE  S LD  +R  M+ ELLRL  +LQ T+++++
Sbjct: 162 AQLSGGMQQRVGLARALSLDPDILLMDEAFSALDPLIRRDMQDELLRLQDDLQKTIVFIS 221

Query: 192 HDQVEAMTMADKVVVLNGGKIEQVGSPLDLYHQPANLFVAGFLGTPKMGFLKGKITRVDS 251
           HD  EA+ + D++V++  G + Q+G+P D+   PA+ +VA F+G       +  +T+V +
Sbjct: 222 HDLDEALKLGDRIVLMRDGAVVQIGTPEDILTNPADDYVARFVG-------EADVTKVLT 274

Query: 252 QGCEVQLDAGTRVSLPLGG-----RHLSVGSAVTLGIRPEHLELAK--PGDCALQVTADV 304
            G  ++      V L + G     R +   +  TL +  E   L      D A ++ A+ 
Sbjct: 275 AGSVMKRSEAVAV-LGIDGPRTALRKMRRNAIATLFVLDERHRLVGLITADDAARLAAEG 333

Query: 305 SERLGSDTFCHVRTASGEA 323
              LGS     + T   EA
Sbjct: 334 VRELGSIVRRDIATVPPEA 352


Lambda     K      H
   0.320    0.137    0.389 

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: 306
Number of extensions: 17
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: 367
Length of database: 397
Length adjustment: 30
Effective length of query: 337
Effective length of database: 367
Effective search space:   123679
Effective search space used:   123679
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 (21.8 bits)
S2: 50 (23.9 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