GapMind for catabolism of small carbon sources

 

Alignments for a candidate for HSERO_RS05255 in Rhizobium leguminosarum bv. trifolii WSM1325

Align ABC-type sugar transport system, permease component protein (characterized, see rationale)
to candidate WP_003562293.1 RLEG_RS23605 ABC transporter permease

Query= uniprot:D8J112
         (347 letters)



>NCBI__GCF_000023185.1:WP_003562293.1
          Length = 354

 Score =  242 bits (617), Expect = 1e-68
 Identities = 135/327 (41%), Positives = 204/327 (62%), Gaps = 28/327 (8%)

Query: 36  KLLAFASLLLMILFFSFASPNFMEVDNLVSILQSTAVNGVLAIACTYVIITSGIDLSVGT 95
           KL  F +L  +I+FF+  +PNF    N++ + +  A+N  LA+  T+VIIT GIDLSVG+
Sbjct: 24  KLRTFIALFAVIIFFAIFAPNFTSTANMILMSKHVALNAFLAMGMTFVIITGGIDLSVGS 83

Query: 96  MMTFCAVMAGVVLTNWGMPLPLG----------IAAAIFFGALSGWISGMVIAKLKVPPF 145
           ++  C ++AG ++  +G+ LP+G          +   +  G L G I+G++I KL V PF
Sbjct: 84  IVGLCGMVAGGLIL-YGIELPIGYTIFFNLFEIVLITVSIGLLIGLINGLLITKLNVAPF 142

Query: 146 IATLGMMMLLKGLSLVISGT--------RPIYFNDTEGFSAIAQDSLIGDLIPSLPIPNA 197
           IATLG + + +GL+L+ S          RP Y   T GF       ++G       +P +
Sbjct: 143 IATLGTLYIARGLALLSSDGQTFPNLVGRPEYA--TTGFDFFGAGRILG-------LPVS 193

Query: 198 VLILFLVAIGASIILNKTVFGRYTFALGSNEEALRLSGVKVDFWKVAVYTFSGAICGIAG 257
           + IL ++A+ A+ +   T  GR+ FA+G NE A R+SG++VD  K+ VY FSG    I G
Sbjct: 194 IWILIVLALLAAYVARSTPIGRHIFAVGGNERAARMSGIRVDVVKIFVYMFSGLCAAIVG 253

Query: 258 LIIASRLNSAQPALGQGYELDAIAAVVIGGTSLSGGTGTILGTIIGAFIMSVLVNGLRIM 317
           ++I+S L +A PA G+ +EL+AIAA V+GGTS+SGG GTI GTIIGAF++ +L +GL +M
Sbjct: 254 VVISSELMAAHPATGESFELNAIAAAVLGGTSMSGGRGTIGGTIIGAFVIGILSDGLVMM 313

Query: 318 SVAQEWQTVVTGVIIILAVYLDILRRR 344
            V+  WQ V+ G++II+AV +D  +RR
Sbjct: 314 GVSSFWQMVIKGLVIIIAVVVDQAQRR 340


Lambda     K      H
   0.326    0.139    0.398 

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: 13
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: 347
Length of database: 354
Length adjustment: 29
Effective length of query: 318
Effective length of database: 325
Effective search space:   103350
Effective search space used:   103350
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 15 ( 7.1 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 40 (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