GapMind for catabolism of small carbon sources

 

Alignments for a candidate for TM1750 in Sinorhizobium meliloti 1021

Align TM1750, component of Probable mannose/mannoside porter. Induced by beta-mannan (Conners et al., 2005). Regulated by mannose-responsive regulator manR (characterized)
to candidate SMa1370 SMa1370 ABC transporter ATP-binding protein

Query= TCDB::Q9X272
         (328 letters)



>FitnessBrowser__Smeli:SMa1370
          Length = 327

 Score =  282 bits (721), Expect = 9e-81
 Identities = 145/296 (48%), Positives = 199/296 (67%), Gaps = 2/296 (0%)

Query: 27  KRILKAVDGISIEIKEGETLGLVGESGCGKSTLGRTILKLLRPDGGKIFFEGKDITNLND 86
           +R + AV  +S ++  GETLGLVGESG GK+T+GR +L+ +    G+I F G+DIT+L  
Sbjct: 27  RRSVNAVSDVSFDLAPGETLGLVGESGSGKTTVGRAVLRRIPAAQGRIVFGGEDITHLGG 86

Query: 87  KEMKPYRKKMQIIFQDPLGSLNPQMTVGRIIEDPLIIHKIGTK-KERRKRVEELLDMVGI 145
           + ++  R +MQI+ QDP  SLNP+M V  I+ +PLI+H +    +E R  V ELL+ VG+
Sbjct: 87  EPLRRLRARMQIVLQDPYTSLNPRMKVSSIVAEPLIVHGLAASAEEARAAVAELLERVGL 146

Query: 146 GREFINSFPHEFSGGQQQRIGIARALALNPKFIVCDEPVSALDVSIQAQIIDLLEEIQQK 205
             +  + +PH FSGGQ+QRIGIARALAL P  IV DEPVSALDVS++AQ+++L++++Q+ 
Sbjct: 147 PGDAADRYPHSFSGGQRQRIGIARALALKPALIVADEPVSALDVSVRAQVVNLMQDLQRD 206

Query: 206 MGISYLFIAHNLAVVEHISHKVAVMYLGKIVEYGDVDKIFLNPIHPYTRALLKSVPKI-P 264
           +GISYLFIAH+LA+V HISH+VA+MY G+IVE    D I+  PIHPYT ALL +VP   P
Sbjct: 207 LGISYLFIAHDLAIVRHISHRVAIMYAGRIVEIAPRDAIYQRPIHPYTEALLSAVPVANP 266

Query: 265 WDGQKQRFYSLKGELPSPIDLPKGCRFQTRCTEKKAICFEKEPELTEVEKNHFVSC 320
              + +R     GE       P GCRF  RC      C E+ P+L     +HF +C
Sbjct: 267 KLQRARRRIVPPGESVDIASPPTGCRFHPRCPLATDRCREEAPQLLRKTGDHFAAC 322


Lambda     K      H
   0.321    0.142    0.417 

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: 311
Number of extensions: 10
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: 328
Length of database: 327
Length adjustment: 28
Effective length of query: 300
Effective length of database: 299
Effective search space:    89700
Effective search space used:    89700
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: 48 (23.1 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