GapMind for catabolism of small carbon sources

 

Alignments for a candidate for glcV in Rhizobium freirei PRF 81

Align monosaccharide-transporting ATPase (EC 3.6.3.17) (characterized)
to candidate WP_004112319.1 RHSP_RS07740 ABC transporter ATP-binding protein

Query= BRENDA::Q97UY8
         (353 letters)



>NCBI__GCF_000359745.1:WP_004112319.1
          Length = 351

 Score =  212 bits (540), Expect = 1e-59
 Identities = 123/364 (33%), Positives = 207/364 (56%), Gaps = 29/364 (7%)

Query: 2   VRIIVKNVSKVFKKGKVVALDNVNINIENGERFGILGPSGAGKTTFMRIIAGLDVPSTGE 61
           +RI++ N SK F   KV+  +N+ + + +GE   +LGPSG GK+T +  + G+  P+ G 
Sbjct: 1   MRILLDNFSKSFGSTKVI--ENMRLEVGSGEMLALLGPSGCGKSTTLFAVCGIHRPTGGR 58

Query: 62  LYFDDRLVASNGKLIVPPEDRKIGMVFQTWALYPNLTAFENIAFPLTNMKMSKEEIRKRV 121
           + F DR V       +P + R +G+VFQ++ALYP++T  ENI FPL    M   EIRK V
Sbjct: 59  ILFGDRDVTD-----LPSQVRNVGVVFQSYALYPHMTVAENIGFPLKVKGMPTAEIRKEV 113

Query: 122 EEVAKILDIHHVLNHFPRELSGGQQQRVALARALVKDPSLLLLDEPFSNLDARMRDSARA 181
           + +A ++ I +++   P ELSGGQQQRVALARAL++ P +LLLDEP +NLDA++R   R+
Sbjct: 114 DRIAALVQIGNLMGRRPAELSGGQQQRVALARALIRKPDVLLLDEPLANLDAKLRLEMRS 173

Query: 182 LVKEVQSRLGVTLLVVSHDPADIFAIADRVGVLVKGKLVQVGKPEDLYDNPVSIQVASLI 241
            ++ +Q   G+T ++V+HD  +  ++ DR+ ++ +G++VQ+  P ++Y++P +  VA  +
Sbjct: 174 EIRRLQRETGITAILVTHDQVEAMSMCDRIAIMKEGEIVQIATPAEMYNDPKTAFVAGFL 233

Query: 242 GE--INELEGKVTNEGVVI--GSLRFPVSVSSD-----RAIIGIRPEDVKLSKDVIKDDS 292
           G   I  L G +     V+    +R P+  + D     + ++G+RPE    + DV     
Sbjct: 234 GNPPITFLRGVMDKGAFVVPESEIRVPLPDAVDASEGTKLMLGVRPEHFTPTGDVAVSGK 293

Query: 293 WILV---GKGKVKVIGYQGGLFRITITPLDSEEEIFTYSDHPIHSGEEVLVYVRKDKIKV 349
                  G+  +  +   GG    +I P+ ++          IH G++V   +    + V
Sbjct: 294 ITFAETQGRENLYDVLLAGGPLLRSIQPVRND----------IHVGDDVRWAIDSRSVLV 343

Query: 350 FEKN 353
           F++N
Sbjct: 344 FDEN 347


Lambda     K      H
   0.319    0.139    0.390 

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: 305
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: 353
Length of database: 351
Length adjustment: 29
Effective length of query: 324
Effective length of database: 322
Effective search space:   104328
Effective search space used:   104328
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 (21.7 bits)
S2: 49 (23.5 bits)

This GapMind analysis is from Sep 24 2021. The underlying query database was built on Sep 17 2021.

Links

Downloads

Related tools

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