GapMind for catabolism of small carbon sources

 

Alignments for a candidate for ytfT in Skermanella stibiiresistens SB22

Align Galactofuranose transporter permease protein YtfT (characterized)
to candidate WP_051511581.1 N825_RS05320 ABC transporter permease

Query= SwissProt::P39328
         (341 letters)



>NCBI__GCF_000576635.1:WP_051511581.1
          Length = 338

 Score =  167 bits (424), Expect = 3e-46
 Identities = 110/332 (33%), Positives = 183/332 (55%), Gaps = 16/332 (4%)

Query: 1   MMPQSLPDTTTPKRRFRWPTGMPQ---LVALLLVLLVDSLVAPHFWQVVLQDGRLFGSPI 57
           + P S     T      W   + Q   ++AL+++L+V SL++P+F    L    +F    
Sbjct: 15  LAPSSKMGAQTGASSINWTRFLVQYSNVLALIVILVVASLLSPYF----LSTRNIF---- 66

Query: 58  DILNRAAPVALLAIGMTLVIATGGIDLSVGAVMAIAGATTAAMTVAGFSLPIVLLSALGT 117
           ++L  A  V ++AIGMT VI   GIDLSVG+++ ++ A TA+   A + + I     L +
Sbjct: 67  NVLRGATMVGIVAIGMTYVILNRGIDLSVGSLVGLSAALTASF--ADYGIGIAASIGLVS 124

Query: 118 GILAGLWNGILVAILKIQPFVATLILMVAGRGVAQLITAGQIVTFNSPD--LSWFGSGSL 175
           G++ GL NG+++  L++QPF+ATL +M+  RG+  + T G  +  + P    +W GS  +
Sbjct: 125 GLVLGLANGLMITKLRLQPFIATLGMMIFARGLVFVYTNGSNIVVDKPTDAFTWLGSAYI 184

Query: 176 LFLPTPVIIAVLTLILFWLLTRKTALGMFIEAVGINIRAAKNAGVNTRIIVMLTYVLSGL 235
             +P PV++ VL   L  L+ R T  G  I AVG N  AA+ +G+N     +  Y +SG+
Sbjct: 185 GPVPVPVVVFVLIWALCALVLRYTVFGREIFAVGANEEAARLSGINVDRNKIRVYCISGV 244

Query: 236 CAAIAGIIVAADIRGADANNAGLWLELDAILAVVIGGGSLMGGRFNLLLSVVGALIIQGM 295
            AA AG+I+A+ +   +  N G   ELDAI A +IGG +  GG  ++  +V+G LI+  +
Sbjct: 245 LAAFAGVIMASRLTVGEP-NGGTLFELDAIAATLIGGTTFDGGVGSVHGTVLGVLILAFL 303

Query: 296 NTGILLSGFPPEMNQVVKAVVVLCVLIVQSQR 327
           +  + L    P    ++K V+++  ++V   R
Sbjct: 304 SNVLNLLNISPYSQMLLKGVIIVLAVVVSEWR 335


Lambda     K      H
   0.327    0.142    0.416 

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: 263
Number of extensions: 15
Number of successful extensions: 4
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: 341
Length of database: 338
Length adjustment: 28
Effective length of query: 313
Effective length of database: 310
Effective search space:    97030
Effective search space used:    97030
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