GapMind for catabolism of small carbon sources

 

Alignments for a candidate for HSERO_RS17020 in Nocardioides daejeonensis MJ31

Align ABC-type sugar transport system, ATPase component protein (characterized, see rationale)
to candidate WP_110206994.1 DNK54_RS11055 ABC transporter ATP-binding protein

Query= uniprot:D8IPI1
         (406 letters)



>NCBI__GCF_003194585.1:WP_110206994.1
          Length = 368

 Score =  236 bits (602), Expect = 8e-67
 Identities = 150/364 (41%), Positives = 213/364 (58%), Gaps = 17/364 (4%)

Query: 2   ADIHCQALAKHYAGGPPVLHPLDLHIGDGEFVVLLGPSGCGKSTMLRMIAGLEDISGGTL 61
           A I    + K Y G   +L+ +DL I  GEF+ LLG SG GKST+L +IAG     GG +
Sbjct: 14  ASIEVDRIRKVY-GSTTILNDIDLDIRAGEFLTLLGASGSGKSTLLNIIAGFIKADGGDV 72

Query: 62  RIGGTVVNDLPARERNVAMVFQNYALYPHMSVYDNIAFGLRRLKRPAAEIDRRVREVAAL 121
           R+ G  +  +PA +R + MVFQ+YAL+PHMSVYDN+A+GLRR   P AEI   V +   +
Sbjct: 73  RVDGKSITSVPAHKRGLGMVFQHYALFPHMSVYDNVAYGLRRHGFPKAEIPGLVADALEM 132

Query: 122 LNLEALLERKPRAMSGGQQQRAAIARAIIKTPSVFLFDEPLSNLDAKLRAQLRGDIKRLH 181
           + +  L +R+P  +SGGQQQR A+ARA++  P V L DEPL  LD  LR QL+ +I+RLH
Sbjct: 133 VEMGHLGKRRPAELSGGQQQRVALARAVVFRPRVLLMDEPLGALDKMLREQLQLEIRRLH 192

Query: 182 QRLRTTTVYVTHDQLEAMTLADRVILMQDGRIVQAGSPAELYRYPRNLFAAGFIGTPAMN 241
           + +  T V+VTHDQ EA+T++DR+ L++ G IVQ G+P ELY  P   +AA FIG    N
Sbjct: 193 KEMGITFVFVTHDQEEALTMSDRIALLEKGDIVQLGTPEELYDAPSCRYAAEFIG--VSN 250

Query: 242 FLSGTVQRQDGQLFIETAHQRWALTGERFSRLRHAMAVKLAVRPDHVRI-AGEREPAA-S 299
            ++G+   + G +F +T +Q    T  + S    A    L VRP+ +R+ AG+  PA   
Sbjct: 251 IMTGS---RAGDVFTDTRNQ----TTHKVSG-GAADGTVLMVRPERLRVSAGQVGPAGHE 302

Query: 300 LTCPVSVELVEILGADAL--LTTRCGDQTL--TALVPADRLPQPGATLTLALDQHELHVF 355
              P  V     LG+D    + T  G++ +  T +   D   QPG  +TL  +  +  V 
Sbjct: 303 NALPAIVSDCVYLGSDRTVHVRTASGEEMVARTEVPRTDDGIQPGVPVTLTWNIEDARVL 362

Query: 356 DVES 359
             E+
Sbjct: 363 AEEA 366


Lambda     K      H
   0.321    0.137    0.403 

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: 418
Number of extensions: 19
Number of successful extensions: 1
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: 406
Length of database: 368
Length adjustment: 30
Effective length of query: 376
Effective length of database: 338
Effective search space:   127088
Effective search space used:   127088
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.4 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 41 (21.8 bits)
S2: 50 (23.9 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