GapMind for catabolism of small carbon sources

 

Alignments for a candidate for HSERO_RS05255 in Collimonas pratensis Ter91

Align ABC-type sugar transport system, permease component protein (characterized, see rationale)
to candidate WP_061936170.1 CPter91_RS01725 ABC transporter permease

Query= uniprot:D8J112
         (347 letters)



>NCBI__GCF_001584185.1:WP_061936170.1
          Length = 327

 Score =  242 bits (617), Expect = 1e-68
 Identities = 136/322 (42%), Positives = 205/322 (63%), Gaps = 15/322 (4%)

Query: 35  QKLLAFASLLLMILFFSFASPNFMEVDNLVSILQSTAVNGVLAIACTYVIITSGIDLSVG 94
           QK  A  SL+++ L FS  S  F  ++N +S+        +L I  T VIIT GIDLSVG
Sbjct: 10  QKFAALGSLVVLGLVFSLTSDAFFTLNNGMSVALQVTSIAILGIGATCVIITGGIDLSVG 69

Query: 95  TMMTFCAVMAGVVLTNWGMPLPLGIAAAIFFGALSGWISGMVIAKLKVPPFIATLGMMML 154
           +++    V+A +V+   GMP+P+G+   +  GA+ G ++G+ I +LK+PPFIATLGMM++
Sbjct: 70  SVLALAGVIAAMVVKA-GMPVPVGMLCGLAVGAVCGGLNGLCITQLKLPPFIATLGMMLV 128

Query: 155 LKGLSLVISGTRPIYFNDTEGFSAIAQDSLIG----------DLI-PSLPIPNAVLILFL 203
            +G++L ++G RP+     E F  +   +L            D++ P +P P  V+++ +
Sbjct: 129 ARGVALQVTGARPVS-GLPEEFGTLGNGTLFRIVKETTGPFPDVVFPGIPYP--VILMVV 185

Query: 204 VAIGASIILNKTVFGRYTFALGSNEEALRLSGVKVDFWKVAVYTFSGAICGIAGLIIASR 263
           +AI  SI+L++T FGR+ +A+GSN EA RLSGVKV    +  Y  SG + G+ G ++ SR
Sbjct: 186 IAIVISIMLSRTQFGRHIYAVGSNAEAARLSGVKVARVTLWTYVISGTLAGLTGCVLMSR 245

Query: 264 LNSAQPALGQGYELDAIAAVVIGGTSLSGGTGTILGTIIGAFIMSVLVNGLRIMSVAQEW 323
           L +AQP  G  YELDAIA+ VIGGTSL GG GTI GT IG+F++ +L NGL +  V+   
Sbjct: 246 LVTAQPNEGVMYELDAIASAVIGGTSLIGGIGTISGTAIGSFVIGILRNGLNMNGVSSFV 305

Query: 324 QTVVTGVIIILAVYLDILRRRR 345
           Q ++ G++I+L V++D +R RR
Sbjct: 306 QQIIIGLVILLTVWIDQMRNRR 327


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: 259
Number of extensions: 11
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: 327
Length adjustment: 28
Effective length of query: 319
Effective length of database: 299
Effective search space:    95381
Effective search space used:    95381
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 Sep 24 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