GapMind for catabolism of small carbon sources

 

Alignments for a candidate for natD in Klebsiella michiganensis M5al

Align NatD, component of The neutral amino acid permease, N-1 (transports pro, phe, leu, gly, ala, ser, gln and his, but gln and his are not transported via NatB) (characterized)
to candidate BWI76_RS05990 BWI76_RS05990 branched-chain amino acid ABC transporter permease

Query= TCDB::Q8YXD0
         (288 letters)



>FitnessBrowser__Koxy:BWI76_RS05990
          Length = 299

 Score =  157 bits (396), Expect = 4e-43
 Identities = 98/289 (33%), Positives = 172/289 (59%), Gaps = 18/289 (6%)

Query: 6   IQLIVNGIAVGSIIALAAVGLTLTYGILRLSNFAHGDFLTLGAYLTFFVNT-----FGVN 60
           +Q +VNG+++G + AL A+G T+ YG+LRL NFAH D + +GA+ T F+ +     FGV 
Sbjct: 7   LQQVVNGMSLGGMYALIAIGYTMVYGVLRLINFAHADVMMVGAFTTLFLFSSIGLPFGVA 66

Query: 61  IWLSMIVAVVGTVGVMLLSEKLLWSRMRSIRANSTTLIIISIGLALFLRNGIILIWGGRN 120
           ++L++  A+ G  G+++  +++ +  +R  +A+  +++I +IG++ FL N   +++GG +
Sbjct: 67  VFLTL--ALCGLFGMLI--DRVAYRPLR--QASKISMLITAIGVSFFLENLFNVLFGGSS 120

Query: 121 QNYNLP-ITPALDIFGVKVPQNQLLVLAL-AVLSIGALHYLLQNTKIGKAMRAVADDLDL 178
           + ++ P        FG  +  N   ++ L  VL + A+ +LL  T+ G A+RAVA D++ 
Sbjct: 121 RFFSAPDFFNNTRAFGDVIITNVAWIVPLITVLLLLAILWLLYRTRYGMAIRAVAFDVNT 180

Query: 179 AKVSGIDVEQVIFWTWLIAGTVTSLGGSMYGL-ITAVRPNMGWFLILPLFASVILGGIGN 237
            ++ GID  ++I   + +  ++ +LGG  Y +    + P MG  + L  FA+ +LGGIG+
Sbjct: 181 VRLMGIDANRIISLVFALGSSLAALGGVFYSISYPTIDPLMGVLIGLKAFAAAVLGGIGS 240

Query: 238 PYGAIAAAFIIGIVQEVST---PFLGSQYKQGVALLIMILVLLIRPKGL 283
             GA+   FI+G  + V+    P LG  YK   A + +ILVLL RP G+
Sbjct: 241 VTGAVLGGFILGFTEVVAVALFPELGG-YKDAFAFMFLILVLLFRPVGI 288


Lambda     K      H
   0.328    0.144    0.426 

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: 261
Number of extensions: 11
Number of successful extensions: 5
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: 288
Length of database: 299
Length adjustment: 26
Effective length of query: 262
Effective length of database: 273
Effective search space:    71526
Effective search space used:    71526
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 15 ( 7.1 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 40 (21.7 bits)
S2: 48 (23.1 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