GapMind for catabolism of small carbon sources

 

Alignments for a candidate for malK in Klebsiella michiganensis M5al

Align Maltose-transporting ATPase (EC 3.6.3.19) (characterized)
to candidate BWI76_RS03270 BWI76_RS03270 sugar ABC transporter ATP-binding protein CymD

Query= reanno::psRCH2:GFF857
         (371 letters)



>FitnessBrowser__Koxy:BWI76_RS03270
          Length = 376

 Score =  345 bits (885), Expect = 1e-99
 Identities = 187/364 (51%), Positives = 243/364 (66%), Gaps = 12/364 (3%)

Query: 1   MASVTLRDICKSYD-GTPITRHIDLDIEDGEFVVFVGPSGCGKSTLLRLIAGLEDITSGD 59
           MA+V+LR I K Y+ G      IDL+I DGEF+VFVGPSGC KST LR+IAGLEDI+ G+
Sbjct: 1   MATVSLRKIEKRYENGFKAVHGIDLEIHDGEFMVFVGPSGCAKSTTLRMIAGLEDISGGE 60

Query: 60  LLIDNQRVNDLPPKDRSVGMVFQSYALYPHMTVAENMAFGLKLASVDKREIKRRVEAVAE 119
           + I N++VNDLPPKDR + MVFQ+YALYPH TV +NMAFGLK+    K EIKRRVE  AE
Sbjct: 61  IYIGNRKVNDLPPKDRGIAMVFQNYALYPHKTVFDNMAFGLKMQKRPKDEIKRRVEDAAE 120

Query: 120 ILQLDKLLERKPKDLSGGQRQRVAIGRTMVREPKVFLFDEPLSNLDAFLRVQMRIEIARL 179
            L++ +LL RKPK++SGGQRQRVA+GR +VR+P VFLFDEPLSNLDA LRV MR++IA+L
Sbjct: 121 KLEITELLYRKPKEMSGGQRQRVAVGRAIVRKPDVFLFDEPLSNLDAKLRVSMRMKIAQL 180

Query: 180 HQRIR-----STMIYVTHDQVEAMTLADKIVVLNAGEIAQVGQPLHLYHYPKNRFVAGFL 234
           H+ ++     +TMIYVTHDQ EA+TL D+I VLN G I QV  P  LY+YP N+FVA F+
Sbjct: 181 HRSLKEEGHPATMIYVTHDQTEALTLGDRICVLNHGNIMQVDTPTDLYNYPNNKFVASFI 240

Query: 235 GSPQMNFVEVRAISASPETVTIELPSGYPLTLPVDGSAVSPG---DPLTLGIRPEHFVMP 291
           GSP +N ++  AI  + E + +E+  G  + +P     +  G    P+  GIRPEH  + 
Sbjct: 241 GSPSINLIDT-AIRKNNERLYVEIAPGVEILIPHSKQVLLEGYINKPVCFGIRPEHISLA 299

Query: 292 DEAD--FTFHGQITVAERLGQYNLLYLTLERLQDVITLCVDGNLRVTEGETFAAGLKADK 349
            + D   TF G +TV E +G    LY  +   + +  +          G+T    L    
Sbjct: 300 SDDDDLNTFEGVLTVVENMGSEKFLYFIVGGKELIARVDTQDINPFHIGKTLRFNLNTAF 359

Query: 350 CHLF 353
           CH+F
Sbjct: 360 CHVF 363


Lambda     K      H
   0.322    0.139    0.405 

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: 416
Number of extensions: 16
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: 371
Length of database: 376
Length adjustment: 30
Effective length of query: 341
Effective length of database: 346
Effective search space:   117986
Effective search space used:   117986
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 (21.9 bits)
S2: 50 (23.9 bits)

This GapMind analysis is from Sep 17 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