GapMind for catabolism of small carbon sources

 

Alignments for a candidate for gntC in Skermanella stibiiresistens SB22

Align TRAP dicarboxylate transport system, periplasmic component (DctP-like) (characterized, see rationale)
to candidate WP_037454475.1 N825_RS17150 DctP family TRAP transporter solute-binding subunit

Query= uniprot:G8AR24
         (337 letters)



>NCBI__GCF_000576635.1:WP_037454475.1
          Length = 326

 Score =  214 bits (545), Expect = 2e-60
 Identities = 117/329 (35%), Positives = 192/329 (58%), Gaps = 7/329 (2%)

Query: 1   MKLLRSVLLATGLAAAILAPVAASAQDIKPRLIRFGYGLSESSNQGRAVKFFVEDMAKRS 60
           MK+ R V  A  LA A L P A     +    ++ G+  + +S+ G A     E++A+RS
Sbjct: 1   MKMTRWVSTAMALALASLLPSANPT--LAATTLQMGHPTASNSHYGVASATLAEELARRS 58

Query: 61  GGKLKVKGFADASLGSDIQMQNALIGGAQEMMVGSTATLVGIVKDFAVFDLPFLFNNEQE 120
            GK K+        G++ +M  +   G  +++V ST  +   V + A+ D+PFLF +   
Sbjct: 59  NGKFKL---VITPNGAEREMVESAQIGTLDLLVTSTGPVGNFVPEVAIVDIPFLFKDYTH 115

Query: 121 ADAVFDGPFGQKLAAKLNDKGLVGLVYWENGFRNLTNSKRPVEKVEDLKGIKLRVMQNPV 180
           A AV DGP GQ +     DKGLV L + ENGFR++TNSK  +    D KG+K+R M+N V
Sbjct: 116 ARAVLDGPVGQDMLKLFPDKGLVALAWGENGFRHITNSKHAINTPADAKGLKVRTMENQV 175

Query: 181 YIDMFNGFGANAVPLSFSELFTAMETGTVDGQENPVTTIQSSKFYEVQKYLTISKHVYSP 240
           ++  F   G    P++F+E+FTA++ GTVDGQENP+  I +SKF +VQKYLT++ HVYSP
Sbjct: 176 HMTAFRQLGVLPTPMAFTEVFTALQQGTVDGQENPIPVITASKFAQVQKYLTLTGHVYSP 235

Query: 241 WIVLASKRWYDGLSADERKIINEAAVASRDFERKDSREASKQSIAYLKDKGMQINELSDA 300
            ++L SK  +DGL+ +E+++  ++A+ +    R+         +A L+  GM++  ++D 
Sbjct: 236 ALILMSKSTFDGLTPEEQQMFRDSAMVAAKAMREKVAAVEATGVAELRAAGMEV--ITDV 293

Query: 301 ELGRMREMVKPAMDKFAADGGADLLNELQ 329
           +  + +E ++PA  ++A   G + +  ++
Sbjct: 294 DRSKFQEALQPAYAEYAKKFGKENIERIR 322


Lambda     K      H
   0.317    0.134    0.372 

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: 225
Number of extensions: 9
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: 337
Length of database: 326
Length adjustment: 28
Effective length of query: 309
Effective length of database: 298
Effective search space:    92082
Effective search space used:    92082
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.3 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.

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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