GapMind for catabolism of small carbon sources

 

Alignments for a candidate for mtlK in Klebsiella michiganensis M5al

Align ABC transporter for D-Sorbitol, ATPase component (characterized)
to candidate BWI76_RS03270 BWI76_RS03270 sugar ABC transporter ATP-binding protein CymD

Query= reanno::BFirm:BPHYT_RS16095
         (369 letters)



>FitnessBrowser__Koxy:BWI76_RS03270
          Length = 376

 Score =  321 bits (822), Expect = 2e-92
 Identities = 182/367 (49%), Positives = 238/367 (64%), Gaps = 17/367 (4%)

Query: 1   MASVTLRNIRKAYDEN-EVMRDINLDIADGEFVVFVGPSGCGKSTLMRMIAGLEDISGGD 59
           MA+V+LR I K Y+   + +  I+L+I DGEF+VFVGPSGC KST +RMIAGLEDISGG+
Sbjct: 1   MATVSLRKIEKRYENGFKAVHGIDLEIHDGEFMVFVGPSGCAKSTTLRMIAGLEDISGGE 60

Query: 60  LTIDGMRVNDVAPAKRGIAMVFQSYALYPHMTLYDNMAFGLKLAGTKKPEIDAAVRNAAK 119
           + I   +VND+ P  RGIAMVFQ+YALYPH T++DNMAFGLK+    K EI   V +AA+
Sbjct: 61  IYIGNRKVNDLPPKDRGIAMVFQNYALYPHKTVFDNMAFGLKMQKRPKDEIKRRVEDAAE 120

Query: 120 ILHIDHLLDRKPKQLSGGQRQRVAIGRAITRKPKVFLFDEPLSNLDAALRVKMRLEFARL 179
            L I  LL RKPK++SGGQRQRVA+GRAI RKP VFLFDEPLSNLDA LRV MR++ A+L
Sbjct: 121 KLEITELLYRKPKEMSGGQRQRVAVGRAIVRKPDVFLFDEPLSNLDAKLRVSMRMKIAQL 180

Query: 180 HDELK-----TTMIYVTHDQVEAMTLADKIVVLSAGNLEQVGSPTMLYHAPANRFVAGFI 234
           H  LK      TMIYVTHDQ EA+TL D+I VL+ GN+ QV +PT LY+ P N+FVA FI
Sbjct: 181 HRSLKEEGHPATMIYVTHDQTEALTLGDRICVLNHGNIMQVDTPTDLYNYPNNKFVASFI 240

Query: 235 GSPKMNFMEGVVQSVTHDGVTVRYETGETQRVAVEPAAVKQG---DKVTVGIRPEHLHVG 291
           GSP +N ++  ++   ++ + V    G    +      + +G     V  GIRPEH+ + 
Sbjct: 241 GSPSINLIDTAIRK-NNERLYVEIAPGVEILIPHSKQVLLEGYINKPVCFGIRPEHISLA 299

Query: 292 MAEDGIS---ARTMAVESLGDAAYLYAESSVAPDGLIARI--PPLERHTKGETQKLGATP 346
             +D ++        VE++G   +LY    V    LIAR+    +     G+T +     
Sbjct: 300 SDDDDLNTFEGVLTVVENMGSEKFLY--FIVGGKELIARVDTQDINPFHIGKTLRFNLNT 357

Query: 347 EHCHLFD 353
             CH+FD
Sbjct: 358 AFCHVFD 364


Lambda     K      H
   0.320    0.135    0.384 

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: 400
Number of extensions: 21
Number of successful extensions: 3
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: 369
Length of database: 376
Length adjustment: 30
Effective length of query: 339
Effective length of database: 346
Effective search space:   117294
Effective search space used:   117294
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: 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