GapMind for catabolism of small carbon sources

 

Alignments for a candidate for glk in Desulfovibrio vulgaris Miyazaki F

Align Glucokinase; EC 2.7.1.2; Glucose kinase (uncharacterized)
to candidate 8500137 DvMF_0900 Glucokinase (RefSeq)

Query= curated2:B2J224
         (341 letters)



>FitnessBrowser__Miya:8500137
          Length = 365

 Score =  100 bits (248), Expect = 8e-26
 Identities = 107/386 (27%), Positives = 156/386 (40%), Gaps = 79/386 (20%)

Query: 4   LLAGDIGGTKTILQLVETSDSQGLHT---------IYQESYHSADFPDLVPIVQQFLIKA 54
           +LA DIGGT +   L E       H          +   +  +A F DL+         A
Sbjct: 3   VLAADIGGTNSRFALYEAGGLARGHVPRPQDRLCAVRLPTAGTASFADLLRRAA-----A 57

Query: 55  NTP----IPEKACFAIAGPIVKNTAKLT--NLAWFLDTE----RLQQELGIPHIYLINDF 104
             P     P     A+AGP V+   + T  N+ W +D +    R      +P + LINDF
Sbjct: 58  EEPGLFTSPALLVLAVAGP-VRGGRRCTPPNIPWAVDLDEPALRAPGMPPLPPVLLINDF 116

Query: 105 AAVGYGI------------------SGLQKQD-------LHPLQV--GKPQPETPIGIIG 137
            A  Y                     G  + D       L+ L V  G P P+ PI ++G
Sbjct: 117 VAQAYACLRPAAPDGPVAPVAPVAPDGPDEPDGPVVPDMLNMLDVLDGHPVPDAPIAVVG 176

Query: 138 AGTGLGQGFLIK---QGNNYQVFPSEGGHADFAPRNEIEFQLLKYLLDKHDIQRISVERV 194
           AGTGLG+  L+     G   +V PSEGGHA F   +E E     ++   H  +++  + V
Sbjct: 177 AGTGLGKCLLLPASGDGMPPRVLPSEGGHALFPFTDEREMAFAAFVR-AHTGRQVIGDLV 235

Query: 195 VSGMGIVAIYQFLRDRKFAAESPDIAQIVRTWEQEAGQEEKSVDPGAAIGTAALEKRDRL 254
           VSG G+  ++ F                        GQ  +  +  A + T A      L
Sbjct: 236 VSGPGLRLLHAF----------------------HTGQWLEPAEVAARLATGAPGADSDL 273

Query: 255 S-EQTLQLFIEAYGAEAGNLALKLLPYGGLYIAGGIAPKILPLIQNSGFLLNFTQKGRMR 313
           +  Q L  F   YG    +  L+ L  GG++I+GG+A     L+ +  F   F Q     
Sbjct: 274 ALPQVLSWFARFYGRACRDYVLETLALGGVFISGGVAAATPALVTHPAFAEAFRQSDTHA 333

Query: 314 PLLEEIPVYIILNPQVGLIGAALCAA 339
            LL  +PV ++ +P  GL+GAAL  A
Sbjct: 334 DLLRAVPVRLVRSPDAGLLGAALYGA 359


Lambda     K      H
   0.320    0.140    0.408 

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: 306
Number of extensions: 19
Number of successful extensions: 4
Number of sequences better than 1.0e-02: 1
Number of HSP's gapped: 3
Number of HSP's successfully gapped: 1
Length of query: 341
Length of database: 365
Length adjustment: 29
Effective length of query: 312
Effective length of database: 336
Effective search space:   104832
Effective search space used:   104832
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: 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