GapMind for catabolism of small carbon sources

 

Alignments for a candidate for ackA in Luteimonas huabeiensis HB2

Align Acetate kinase; EC 2.7.2.1; Acetokinase (uncharacterized)
to candidate WP_024889936.1 Z164_RS0106650 hypothetical protein

Query= curated2:Q6N143
         (398 letters)



>NCBI__GCF_000559025.1:WP_024889936.1
          Length = 367

 Score =  216 bits (550), Expect = 9e-61
 Identities = 143/383 (37%), Positives = 199/383 (51%), Gaps = 28/383 (7%)

Query: 5   LLVLNAGSSSIKFALYEAHTEPTADHLICEGGIGSLGHRPHFKVVNSDGSTRYDTYLPEG 64
           LL LN GSS++K A Y  +TE               GH    +++      R    +P G
Sbjct: 6   LLALNVGSSTLKGASYLFNTE---------------GHGAQSRLLE-----RSRAEIPVG 45

Query: 65  TSHDDAMAVLIGWIETTFPEHRLSAVGHRVVHGGALFDGPVDVTPEVIAQLRAFDRLAPL 124
               + +A L+  +   +P      V HR+VHGG L D   ++   V+A+L      APL
Sbjct: 46  VDAQERLATLLEALSEPWPSP--DVVVHRIVHGGDLHDAR-ELDETVLAKLDELVPFAPL 102

Query: 125 HQPHNVSAIEALAKLHPSLPQIACFDTAFHHRLPEVATAFALPRELTEQGVRRYGFHGLS 184
           HQP  ++   A     P   Q   FDT FH  L   +    +P      G+RRYGFHGL+
Sbjct: 103 HQPVALAFARAARLRWPHARQGVAFDTDFHASLAPWSRRLPVPEAWDALGIRRYGFHGLA 162

Query: 185 YEYIAGRLPDVAGQAVADGRVVVAHLGAGASMCAMLRCRSIATTMGFTALDGLMMGSRCG 244
           +   A R+       +  GR V AHLG G S+CA+   RS  TTM  T L G+   +R G
Sbjct: 163 FAS-ALRILASHDAGILKGRAVFAHLGGGCSVCAVEGGRSRDTTMALTPLGGIPSPTRSG 221

Query: 245 ELDPGVVLYLLEEKSMTAREIEDLLYRESGLLGVSGISDDMRTLLASDDPHACEAIELFV 304
           +LDPG +LYLL  + + A+ +E+ LYR +GL G++G   DMR LL    P A  A+ELF 
Sbjct: 222 DLDPGALLYLLRHERLDAQALENGLYRSAGLAGIAG-HGDMRVLLTDPGPQAQLAVELFA 280

Query: 305 YRIARELGSLAAALGGLDALVFTGGIGEHASEIRRRVCEQAAWLGVTLDPDANASLSGAG 364
            RIA+ + ++A A+GGLD +VF+GGIG  A  +R R+  + AWLG+ L PD N   +GA 
Sbjct: 281 VRIAQSIAAMATAIGGLDHVVFSGGIGHRAPVLRARIVARLAWLGLALAPDVND--AGAT 338

Query: 365 RISAPDSKVSAWAIPTDEDLMIA 387
           RI       S W +  DE+  +A
Sbjct: 339 RIDRGGGP-SIWNVAIDEERELA 360


Lambda     K      H
   0.321    0.137    0.413 

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: 431
Number of extensions: 33
Number of successful extensions: 5
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: 398
Length of database: 367
Length adjustment: 30
Effective length of query: 368
Effective length of database: 337
Effective search space:   124016
Effective search space used:   124016
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 (21.9 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