GapMind for catabolism of small carbon sources

 

Alignments for a candidate for mtlK in Derxia gummosa DSM 723

Align ABC transporter for D-mannitol and D-mannose, ATPase component (characterized)
to candidate WP_028312315.1 H566_RS0116635 ABC transporter ATP-binding protein

Query= reanno::pseudo3_N2E3:AO353_25895
         (367 letters)



>NCBI__GCF_000482785.1:WP_028312315.1
          Length = 358

 Score =  233 bits (593), Expect = 8e-66
 Identities = 140/329 (42%), Positives = 208/329 (63%), Gaps = 17/329 (5%)

Query: 4   LKIKNLQKGFEGFSIIKGIDLEVNDREFVVFVGPSGCGKSTLLRLIAGLEEVTAGTIELD 63
           L + +L+  +    I+KG+ ++++  E +  +GPSG GK+TLLR +AGLE+   G I + 
Sbjct: 7   LTVTDLKLSYGDNPILKGVSMDLHRGEVISLLGPSGSGKTTLLRAVAGLEQPHEGRISIA 66

Query: 64  GRDI------TEVSPAKRDLAMVFQTYALYPHMSVRKNMSFALDLAGVNKAEVEKKVNEA 117
           G+++       EV   +R+L +VFQ+YAL+PH +V  N+++ L L   + A ++ +V++A
Sbjct: 67  GKNVFDGAAGVEVPAEQRNLGLVFQSYALWPHKTVFDNVAYGLKLRKTDSATIKDRVSDA 126

Query: 118 ARILELGPMLERKPKQLSGGQRQRVAIGRAIVRNPKIFLFDEPLSNLDAALRVQMRLELA 177
            + L LG + ER P QLSGGQ+QRVAI RA+V NP + L DEPLSNLDA LR + R  L 
Sbjct: 127 LKNLGLGHLGERYPHQLSGGQQQRVAIARALVYNPPVILLDEPLSNLDAKLREEARAWLR 186

Query: 178 RLHKELQATMIYVTHDQVEAMTLADKVVVLNGGRIEQVGSPLELYHQPANLFVAGFLGTP 237
            L   LQ + + VTHDQ EAM ++D++++LNGGRIEQ GSP E+Y +PA+LF AGF+GT 
Sbjct: 187 ELIVRLQLSALVVTHDQGEAMAMSDRILLLNGGRIEQQGSPTEMYLKPASLFAAGFMGTN 246

Query: 238 KMGFLKGKVTRVERQNC-EVLLDAGTRITLPLS---GANLSIGGAVTLGIRPEHLNLA-L 292
               LKG   R+E++N  ++LLD G       +   GA  ++GG  T  +R E + LA  
Sbjct: 247 NT--LKG---RIEQRNADDILLDIGEHKLWGRACGQGAPATVGGEATAVVRVEGVKLADG 301

Query: 293 PGDCTLQVTADVSERLGSDTFCHVLTASG 321
           PG   + +    S  LG D + +VL ++G
Sbjct: 302 PGPNRMPMDLVTSMYLG-DRWEYVLDSAG 329


Lambda     K      H
   0.321    0.137    0.390 

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: 325
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: 367
Length of database: 358
Length adjustment: 29
Effective length of query: 338
Effective length of database: 329
Effective search space:   111202
Effective search space used:   111202
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: 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