GapMind for catabolism of small carbon sources

 

Alignments for a candidate for malK_Aa in Klebsiella michiganensis M5al

Align ABC-type maltose transporter (EC 7.5.2.1) (characterized)
to candidate BWI76_RS26290 BWI76_RS26290 glycerol-3-phosphate ABC transporter ATP-binding protein

Query= BRENDA::Q70HW1
         (384 letters)



>FitnessBrowser__Koxy:BWI76_RS26290
          Length = 356

 Score =  330 bits (845), Expect = 5e-95
 Identities = 174/366 (47%), Positives = 244/366 (66%), Gaps = 15/366 (4%)

Query: 1   MARVLLEHIYKTYPGQTEPTVKDFNLDIQDKEFTVFVGPSGCGKTTTLRMIAGLEDITEG 60
           MA + L+ + K++ G+T+  ++   LD+ D EF V VGPSGCGK+T LRM+AGLE +T G
Sbjct: 1   MAGLKLQAVTKSWDGKTQ-VIQPLTLDVADGEFIVMVGPSGCGKSTLLRMVAGLERVTSG 59

Query: 61  NLYIGDRRVNDVPPKDRDIAMVFQNYALYPHMTVYQNMAFGLKLRKVPKAEIDRRVQEAA 120
           +++I  +RV ++ PKDR IAMVFQNYALYPHM+V +NMA+GLK+R + K  I  RVQEAA
Sbjct: 60  DIWIDRKRVTEMEPKDRGIAMVFQNYALYPHMSVEENMAWGLKIRGLGKGLIAERVQEAA 119

Query: 121 KILDIAHLLDRKPKALSGGQRQRVALGRAIVREPQVFLMDEPLSNLDAKLRVQMRAEIRK 180
           +IL++  LL R+P+ LSGGQRQRVA+GRAIVR+P VFL DEPLSNLDAKLRVQMR E++ 
Sbjct: 120 RILELDGLLKRRPRELSGGQRQRVAMGRAIVRDPAVFLFDEPLSNLDAKLRVQMRLELQH 179

Query: 181 LHQRLQTTVIYVTHDQTEAMTMGDRIVVMRDGVIQQADTPQVVYSQPKNMFVAGFIGSPA 240
           LH+RL+TT +YVTHDQ EAMT+  R++VM  GV +Q  TP  VY +P + FVA FIGSPA
Sbjct: 180 LHRRLKTTSLYVTHDQVEAMTLAQRVMVMNKGVAEQIGTPVEVYEKPASRFVASFIGSPA 239

Query: 241 MNFIRGEIVQDGDAFYFRAPS-ISLRLPEGRYGVLKASGAIGKPVVLGVRPEDLHDEEVF 299
           MN + G +  DG  F       + +     RY         G+ + LG+RP     E   
Sbjct: 240 MNLLEGRVSDDGSRFELAGGMLLPINSEHRRYA--------GRKMTLGIRP-----EHFA 286

Query: 300 MTTYPDSVLQMQVEVVEHMGSEVYLHTSIGPNTIVARVNPRHVYHVGSSVKLAIDLNKIH 359
           +++  +  + + ++ +E +G++   H   G   +V R+  +     GS++ L +    +H
Sbjct: 287 LSSQAEGGVPLVMDTLEILGADNLAHGRWGEQKLVVRLPHQQRPQAGSTLWLHLPQESLH 346

Query: 360 IFDAET 365
           +FD+ET
Sbjct: 347 LFDSET 352


Lambda     K      H
   0.321    0.138    0.395 

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: 404
Number of extensions: 22
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: 384
Length of database: 356
Length adjustment: 30
Effective length of query: 354
Effective length of database: 326
Effective search space:   115404
Effective search space used:   115404
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 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