GapMind for catabolism of small carbon sources

 

Alignments for a candidate for kdgK in Megamonas funiformis YIT 11815

Align 2-dehydro-3-deoxygluconokinase; 2-keto-3-deoxygluconokinase; 3-deoxy-2-oxo-D-gluconate kinase; KDG kinase; EC 2.7.1.45 (characterized)
to candidate WP_008538927.1 HMPREF9454_RS07600 sugar kinase

Query= SwissProt::P50845
         (324 letters)



>NCBI__GCF_000245775.1:WP_008538927.1
          Length = 313

 Score =  267 bits (682), Expect = 3e-76
 Identities = 139/313 (44%), Positives = 197/313 (62%), Gaps = 2/313 (0%)

Query: 1   MKLDAVTFGESMAMFYANEYGGLHEVSTFSKGLAGAESNVACGLARLGFRMGWMSKVGND 60
           M+   +  GE M +  A   G L+ VS++   +AGAE NVA G ARL  ++ +M+K+G+D
Sbjct: 1   MQSGLILVGEPMGLLIAQTEGSLNNVSSYDLAVAGAEFNVAIGTARLEHKVTYMTKLGDD 60

Query: 61  QLGTFILQELKKEGVDVSRVIRSQDENPTGLLLKSKVKEGDPQVTYYRKNSAASTLTTAE 120
             G  I   LK   +     I    E  TG +LK +   GDP++ Y+RKNSAASTL   +
Sbjct: 61  PFGKRITTVLKDNKIG-DEFISFSKERATGFMLKGRTSVGDPEIFYFRKNSAASTLNEDD 119

Query: 121 YPRDYFQCAGHLHVTGIPPALSAEMKDFTYHVMNDMRNAGKTISFDPNVRPSLWPDQATM 180
             +      G++H+TGI PALS + K  T+ ++   +  G  ISFDPN+RP LW  Q  M
Sbjct: 120 VEKIDLSNYGYIHLTGILPALSEDTKKATFSLIKKAKKQGLFISFDPNLRPQLWKSQEEM 179

Query: 181 VHTINDLAGLADWFFPGIAEGELLTGEKTPEGIADYYLKKGASFVAIKLGKEGAYFKTGT 240
           + TIN+LA  AD   PG AEG++L G    + I D+YL+ GAS    K G +GAY  T  
Sbjct: 180 IQTINELASYADLVLPGQAEGKILIGTDDEKEINDFYLQNGASICVTKCGSKGAYVSTKD 239

Query: 241 SEGFL-EGCRVDRVVDTVGAGDGFAVGVISGILDGLSYKDAVQRGNAIGALQVQAPGDMD 299
            EG++ EG +V++VVDTVGAGDGFA GV++G+++GL+  +AV+RG AIGA+QV + GD +
Sbjct: 240 GEGYMVEGYKVEKVVDTVGAGDGFATGVVTGLMEGLTLSEAVKRGTAIGAIQVMSRGDNE 299

Query: 300 GLPTREKLASFLS 312
           GLPTR++L  F++
Sbjct: 300 GLPTRQELKDFMN 312


Lambda     K      H
   0.317    0.135    0.399 

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: 324
Number of extensions: 19
Number of successful extensions: 3
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: 324
Length of database: 313
Length adjustment: 27
Effective length of query: 297
Effective length of database: 286
Effective search space:    84942
Effective search space used:    84942
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 (21.6 bits)
S2: 48 (23.1 bits)

This GapMind analysis is from Sep 24 2021. The underlying query database was built on Sep 17 2021.

Links

Downloads

Related tools

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