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_075386538.1 BK574_RS02545 sugar kinase

Query= SwissProt::P50845
         (324 letters)



>NCBI__GCF_002019605.1:WP_075386538.1
          Length = 321

 Score =  227 bits (579), Expect = 3e-64
 Identities = 133/316 (42%), Positives = 186/316 (58%), Gaps = 14/316 (4%)

Query: 2   KLDAVTFGESMAMFYANEYGGLHEVSTFSKGLAGAESNVACGLARLGFRMGWMSKVGNDQ 61
           KLD VTFGE+M +F   +   L  V  F K + GAESNVA GL+RLG  +GW SK+G+D 
Sbjct: 3   KLDVVTFGETMVLFQPEQMQPLEYVYEFPKRIGGAESNVAIGLSRLGHTVGWFSKLGDDP 62

Query: 62  LGTFILQELKKEGVDVSRVIRSQDENPTGLLLKSKVKEGDPQVTYYRKNSAASTLTTAEY 121
            G +IL+ ++ EGV+ S  + ++ E PTGL+ K ++   D  V YYRK SAAS L T + 
Sbjct: 63  FGRYILKSIRGEGVETSSCLFTK-EAPTGLIFKERLSPEDVNVYYYRKGSAASLLETTDL 121

Query: 122 PRDYFQCAGHLHVTGIPPALS-----AEMKDFTYHVMNDMRNAGKTISFDPNVRPSLWP- 175
             +Y   A  LH+TGI PALS     A MK       N M+     I FDPN+R  LW  
Sbjct: 122 DEEYIANAKILHLTGITPALSDTCYQAVMKSIEIAKKNKMK-----IVFDPNLRLKLWSL 176

Query: 176 DQATMVHTINDLAGLADWFFPGIAEGELLTGEKTPEGIADYYLKKGASFVAIKLGKEGAY 235
           ++A  V  +N++A  +D   PG+ EG+ +TG+   E +A+  +      + +KLG +GAY
Sbjct: 177 EKAKQV--LNEIASHSDVILPGLDEGQFMTGKTEIEEVAEALMGGEDKTIIMKLGSKGAY 234

Query: 236 FKTGTSEGFLEGCRVDRVVDTVGAGDGFAVGVISGILDGLSYKDAVQRGNAIGALQVQAP 295
             T   +  +EG  V ++VD VGAGDGFA G++SG+L        V+R NAIGA+ V   
Sbjct: 235 LHTKDEQETIEGYPVTQIVDPVGAGDGFAAGILSGLLREEPLPIVVKRANAIGAMVVGMT 294

Query: 296 GDMDGLPTREKLASFL 311
           GD++GLPT   +  F+
Sbjct: 295 GDIEGLPTLAAVEQFM 310


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: 285
Number of extensions: 9
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: 321
Length adjustment: 28
Effective length of query: 296
Effective length of database: 293
Effective search space:    86728
Effective search space used:    86728
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 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