GapMind for catabolism of small carbon sources

 

Alignments for a candidate for kdgK in Alkalihalobacterium alkalinitrilicum DSM 22532

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_078429240.1 BK574_RS15635 sugar kinase

Query= SwissProt::P50845
         (324 letters)



>NCBI__GCF_002019605.1:WP_078429240.1
          Length = 338

 Score =  244 bits (623), Expect = 2e-69
 Identities = 145/319 (45%), Positives = 194/319 (60%), Gaps = 8/319 (2%)

Query: 4   DAVTFGESMAMFYANEYGGLHEVSTFSKGLAGAESNVACGLARLGFRMGWMSKVGNDQLG 63
           + +T GE+M +F   +   L   S+ +K LAGAESNV+ GL RLG R+GW+S++GND  G
Sbjct: 21  EILTLGETMVLFQTVQDSRLQYASSLAKSLAGAESNVSIGLTRLGKRVGWLSRLGNDPFG 80

Query: 64  TFILQELKKEGVDVSRVIRSQDENPTGLLLKSKVKEGDPQVTYYRKNSAASTLTTAEYPR 123
            +I   L  EGVD+S V R + + PTG++ K      DP V YYRK+SAAS   + E  +
Sbjct: 81  DYIYSTLLGEGVDLSYVRRDK-QYPTGVMFKEIKGAIDPGVYYYRKSSAASVWKSKELSQ 139

Query: 124 DYFQCAGHLHVTGIPPALSAEMKDFTYHVMNDMRNAGKTISFDPNVRPSLWPDQATMVHT 183
           + F+    LH+TGI PALS+E K+ ++  +   + AG  ISFDPN+R  LW   A    T
Sbjct: 140 EMFEGVKTLHLTGITPALSSECKETSFEAIRLAKQAGAMISFDPNMRYKLW-SAAEARQT 198

Query: 184 INDLAGLADWFFPGIAEGELLTGEKTPEGIADYYLKKGASFVAIKLGKEGAYFKTGTSEG 243
             +L  L+D   PGI EGEL+TG++ P+ IA   L  GA  V IK+G EG+   T   EG
Sbjct: 199 FIELIKLSDIILPGIDEGELITGKQDPDSIAIDILALGAKIVVIKVGPEGSIAYT-KEEG 257

Query: 244 FL-----EGCRVDRVVDTVGAGDGFAVGVISGILDGLSYKDAVQRGNAIGALQVQAPGDM 298
            L      G  V +VVDTVGAGDGFA G +S  LD  +  D +QR NAIGA+  Q  GD 
Sbjct: 258 NLYKVKAPGFPVHQVVDTVGAGDGFAAGFLSAYLDQENMFDCLQRANAIGAMVTQYRGDW 317

Query: 299 DGLPTREKLASFLSAQRTV 317
           +GLPT E++ SF+S +  V
Sbjct: 318 EGLPTLEEVESFISGRVAV 336


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: 310
Number of extensions: 10
Number of successful extensions: 4
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: 338
Length adjustment: 28
Effective length of query: 296
Effective length of database: 310
Effective search space:    91760
Effective search space used:    91760
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: 49 (23.5 bits)

This GapMind analysis is from Apr 09 2024. 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