GapMind for catabolism of small carbon sources

 

Alignments for a candidate for scrK in Sedimenticola selenatireducens DSM 17993

Align Fructokinase; D-fructose kinase; Manno(fructo)kinase; EC 2.7.1.4 (characterized)
to candidate WP_029133935.1 A3GO_RS0114065 hypothetical protein

Query= SwissProt::P23917
         (302 letters)



>NCBI__GCF_000428045.1:WP_029133935.1
          Length = 303

 Score =  338 bits (868), Expect = 7e-98
 Identities = 163/301 (54%), Positives = 209/301 (69%), Gaps = 3/301 (0%)

Query: 1   MRIGIDLGGTKTEVIALGDAGEQLYRHRLPTPRDDYRQTIETIATLVDMAEQATGQRGTV 60
           MRIG+DLGGTK E IAL D G  L R R+PTP  DY  T++ +ATL+   EQ TG  G+V
Sbjct: 1   MRIGVDLGGTKIEAIALDDRGNSLTRQRIPTPTGDYHATLDAVATLIGRIEQLTGMHGSV 60

Query: 61  GMGIPGSISPYTGVVKNANSTWLNGQPFDKDLSARLQREVRLANDANCLAVSEAVDGAAA 120
           G+G PGS SP TG+++NANST LNGQP  ++    L R VRLANDA+C A+SE++DGA  
Sbjct: 61  GIGTPGSPSPATGLIRNANSTCLNGQPLQQNFERLLNRPVRLANDADCFALSESIDGAGQ 120

Query: 121 GAQTVFAVIIGTGCGAGVAFNGRAHIGGNGTAGEWGHNPLPWMDEDELRYREEVPCYCGK 180
           G  +VF VIIGTG GAG+  NG      N  AGEWGHNPLPW    E        CYCGK
Sbjct: 121 GFHSVFGVIIGTGVGAGIVINGSLIPHANRIAGEWGHNPLPWPSATE---SPGEACYCGK 177

Query: 181 QGCIETFISGTGFAMDYRRLSGHALKGSEIIRLVEESDPVAELALRRYELRLAKSLAHVV 240
           +GCIETF+SG G  +DYRR +G  + G E+ + +E+ +  AE  + RYE RLA+SLA V+
Sbjct: 178 KGCIETFLSGAGLHLDYRRETGLEISGPELSKRLEQQEQAAERVMARYENRLARSLATVI 237

Query: 241 NILDPDVIVLGGGMSNVDRLYQTVGQLIKQFVFGGECETPVRKAKHGDSSGVRGAAWLWP 300
           N+LDP+VIVLGGG+SN+ RLY+ + ++  +++F     T +   +HGDSSGVRGAAWLWP
Sbjct: 238 NLLDPEVIVLGGGLSNLVRLYERIPRIWAEYIFSDVVRTRLLPPRHGDSSGVRGAAWLWP 297

Query: 301 Q 301
           +
Sbjct: 298 E 298


Lambda     K      H
   0.318    0.137    0.418 

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: 337
Number of extensions: 16
Number of successful extensions: 2
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: 302
Length of database: 303
Length adjustment: 27
Effective length of query: 275
Effective length of database: 276
Effective search space:    75900
Effective search space used:    75900
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 (21.7 bits)
S2: 48 (23.1 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