GapMind for catabolism of small carbon sources

 

Alignments for a candidate for dctP in Magnetovibrio blakemorei MV-1

Align Monocarboxylate 2-oxoacid-binding periplasmic protein all3028; Extracellular solute-binding protein; Extracytoplasmic solute receptor protein all3028; TRAP transporter monocarboxylate 2-oxoacid-binding subunit P (characterized)
to candidate WP_069956584.1 BEN30_RS01590 TRAP transporter substrate-binding protein

Query= SwissProt::Q8YSQ6
         (364 letters)



>NCBI__GCF_001746755.1:WP_069956584.1
          Length = 379

 Score =  278 bits (712), Expect = 1e-79
 Identities = 151/367 (41%), Positives = 213/367 (58%), Gaps = 11/367 (2%)

Query: 1   MKRREVLNTAAIATATTALVSCTQTNTSS----VQAGLPNV-----RWRMTTSWPKSL-G 50
           MKRR+ +  AA+A    AL +C +   ++    V    P +     + +M T+WPK   G
Sbjct: 1   MKRRDFVKGAALAAGAAALTACGKEEQAAAPKEVAPAAPALSKQLRQLKMVTTWPKGFPG 60

Query: 51  TFIGAETVAKRVAEMTNGRFKITPFAAGELVPGLQVLDAVQAGTVECGHTSSYYYIGKSP 110
              GA+ +A  ++ MT GR  +  +  GELVP L+  +AV +GT +  H + YY+ G S 
Sbjct: 61  VGTGAQRLADSISAMTEGRISVKLYGGGELVPALESFNAVSSGTADMYHGAEYYWQGNSK 120

Query: 111 ALAFATSVPFGLNAQQQYAWLYQGGGLAAIQKIYANFNVINFPAGSTGAQMGGWFKKEIK 170
           A  F T+VPFGL A +  AWLY GGG     ++ A FNV  F AG+TG QMGGWF KEI 
Sbjct: 121 AFNFFTTVPFGLTATEMDAWLYYGGGQDLWDELAAGFNVKAFAAGNTGVQMGGWFNKEIN 180

Query: 171 SVSDLKGLKMRIPGLGGQVMSRLGVNVQVLPGGEIYLALDRGAIDAAEWVGPYDDEKLGL 230
           +V D KGLKMR+PGLGG+V+ +LG      P  EI+ AL  GAIDA EWVGP++D  +G 
Sbjct: 181 TVEDYKGLKMRMPGLGGEVIRQLGGQSITTPASEIFSALQSGAIDATEWVGPWNDLAMGF 240

Query: 231 NKAAQFYYYPGWWEPGPTLDVLVNLNAWNRLPKEYQEIFKTATVEANLTMLNQYDALNGE 290
            K A++YYYPG+ EPG TL   +N   WN    + Q I   A    N  ML +++A NG 
Sbjct: 241 YKVAKYYYYPGFHEPGSTLSCGINTTVWNSFSAQDQAIVAFACAAENNRMLAEFNANNGG 300

Query: 291 ALTRLL-AGGTKLVPYSQEIMQAAQKISFDIFEENASKDAAFKQVYEQWKAFRKQIFAWN 349
           AL  L+   G +L   S +I++A  + S  +  E AS D   +++Y+ + +FRKQ   W 
Sbjct: 301 ALKTLVEEHGVQLRRQSDDILKALGEASGVVLAEVASSDPMTRKIYDSFMSFRKQALDWT 360

Query: 350 RVNELSY 356
             +E+++
Sbjct: 361 SKSEMAF 367


Lambda     K      H
   0.317    0.132    0.397 

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: 444
Number of extensions: 26
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: 364
Length of database: 379
Length adjustment: 30
Effective length of query: 334
Effective length of database: 349
Effective search space:   116566
Effective search space used:   116566
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