GapMind for catabolism of small carbon sources

 

Alignments for a candidate for TM1749 in Sinorhizobium meliloti 1021

Align TM1749, component of Probable mannose/mannoside porter. Induced by beta-mannan (Conners et al., 2005). Regulated by mannose-responsive regulator manR (characterized)
to candidate SMc03125 SMc03125 transport system ATP-binding ABC transporter protein

Query= TCDB::Q9X271
         (324 letters)



>FitnessBrowser__Smeli:SMc03125
          Length = 337

 Score =  278 bits (711), Expect = 1e-79
 Identities = 142/314 (45%), Positives = 204/314 (64%), Gaps = 5/314 (1%)

Query: 3   ELLNVNNLKVEFHRVEGIVKAVDGISYKLNKGESLGIVGESGSGKSVSVLSLLRLINRNG 62
           +L+ + +LKV F  V+     + GI   + KGE++G+VGESG GKSV+ L+ L L+    
Sbjct: 7   DLVALRDLKVAFDGVQ----VLHGIDLNVAKGEAVGLVGESGCGKSVTWLAALGLLPGKA 62

Query: 63  RIVDGEAIFLGKDLLKLNKEELRNIRGKDISIIFQNPMTSLNPIIRVGIQVMEPIIWHRL 122
            +  G     G++L    +  L  +RG  I++IFQ+P +SLNP++R+G Q++E +  HR 
Sbjct: 63  AVT-GSVRIDGRELCGARRTALEEVRGGRIAMIFQDPSSSLNPVLRIGRQIVEALYIHRG 121

Query: 123 MKNEEARERAIELLERVGIPESPKRFLNYPFQFSGGMRQRVMIAMALACHPKLLIADEPT 182
           ++ + AR  A+ L++ VGIP++ +RF  YP +FSGG  QR+MIAMALA  P LLIADEPT
Sbjct: 122 LRGDAARVEALRLMDMVGIPDAARRFDLYPHEFSGGQCQRLMIAMALAGEPDLLIADEPT 181

Query: 183 TALDVTIQAQIMELLQELKEEYGMSVIFITHDLSVATNFCDRIITMYAGKIVEEAPVEEI 242
           TALD TIQAQI++LL  L+ E GM+++FI+HDL   +  CDR+  MYAG+IVEE  V ++
Sbjct: 182 TALDATIQAQILDLLNTLRAETGMALVFISHDLGAVSQVCDRVCVMYAGRIVEEGSVAQL 241

Query: 243 LKTPLHPYTKGLLNSTLEIGSRGKKLVPIPGNPPNPTKHPSGCKFHPRCSFAMEICQREE 302
              P HPYT+GL ++   I     +L+PIPG  PNP   P+GC F PRC  A++ C  + 
Sbjct: 242 FSEPRHPYTRGLFDAIPRIDGPRDRLIPIPGTVPNPKHLPAGCSFSPRCPRAVDACGSDY 301

Query: 303 PPLVNISENHRVAC 316
           P L    +  R+AC
Sbjct: 302 PHLEPQGDGRRLAC 315


Lambda     K      H
   0.320    0.139    0.401 

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: 298
Number of extensions: 11
Number of successful extensions: 1
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: 324
Length of database: 337
Length adjustment: 28
Effective length of query: 296
Effective length of database: 309
Effective search space:    91464
Effective search space used:    91464
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: 49 (23.5 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