GapMind for catabolism of small carbon sources

 

Alignments for a candidate for dgoK in Collimonas arenae Ter10

Align 2-keto-3-deoxygalactonate kinase protein; EC 2.7.1.58 (characterized, see rationale)
to candidate WP_061534659.1 CAter10_RS19055 2-dehydro-3-deoxygalactonokinase

Query= uniprot:D8J0Z3
         (319 letters)



>NCBI__GCF_001584165.1:WP_061534659.1
          Length = 335

 Score =  327 bits (837), Expect = 3e-94
 Identities = 177/323 (54%), Positives = 212/323 (65%), Gaps = 14/323 (4%)

Query: 10  LIALDWGTSSLRCYRYDGSGQVVERRAHPWGIMNLPAVEHGDDAQAPYRAALEAACGDWI 69
           LIALDWGTSSLR YR    GQ +E RA PWG+M LP    G   +  + AA E ACGDW+
Sbjct: 10  LIALDWGTSSLRAYRLGTGGQTLEMRALPWGVMQLPETVAGAGEKDGFEAAFEQACGDWL 69

Query: 70  AAAPEAALIAAGMVGSKQGWREAAYLTVPLAPDGIGRKLTEVDTGLGRSLWIIPGLLQNS 129
            AAP   +IAAGMVGS+QGW EA YL+VP+A   IG  L+ V    G+ + I+PGL+QN 
Sbjct: 70  QAAPATPVIAAGMVGSRQGWLEAPYLSVPIAVADIGGNLSIVRNRQGQLIHIVPGLIQNV 129

Query: 130 ALPNVMRGEETQVIGAL-----QQQRQSELLIGLPGTHSKWVRV----VEGRIEHFDTFM 180
            LPNVMRGEETQV+G L     Q   Q E+LIGLPGTHSKWV++     +  + HFDTFM
Sbjct: 130 LLPNVMRGEETQVVGVLSALGKQATLQDEILIGLPGTHSKWVQIRRTDAQAELTHFDTFM 189

Query: 181 TGEVYGALCGHTILGRTMHKPD--VPDDAAFVRGARVAQGPQGQAGVLSNIFSSRTLGLT 238
           TGEV+ ALCGHTILGR M   +       AF RG RV Q   G+AGVLS IFS+RTLGLT
Sbjct: 190 TGEVFAALCGHTILGRGMQTTENVHASATAFERGLRVPQTAAGRAGVLSTIFSTRTLGLT 249

Query: 239 GELAPEAQPDYLSGLLIGHEIAALKSL---YPAQQAPIVLIGDAGLCRRYRLALELYGLG 295
           GEL    Q +YLSGLLIGHEI+AL+ L   +  Q + ++L+G++ LC RY   L  YG  
Sbjct: 250 GELDGTGQREYLSGLLIGHEISALQDLLRQHERQPSRVILVGESALCERYASVLRAYGFA 309

Query: 296 PVSEADAATEAGLWILARHAGLV 318
                  ATE GLW LA  AGL+
Sbjct: 310 RTDVMAQATERGLWQLALTAGLL 332


Lambda     K      H
   0.320    0.137    0.423 

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: 391
Number of extensions: 11
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: 319
Length of database: 335
Length adjustment: 28
Effective length of query: 291
Effective length of database: 307
Effective search space:    89337
Effective search space used:    89337
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: 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