GapMind for catabolism of small carbon sources

 

Alignments for a candidate for malK_Aa in Cupriavidus basilensis 4G11

Align ABC-type maltose transporter (EC 7.5.2.1) (characterized)
to candidate RR42_RS22875 RR42_RS22875 ABC transporter

Query= BRENDA::Q70HW1
         (384 letters)



>FitnessBrowser__Cup4G11:RR42_RS22875
          Length = 351

 Score =  261 bits (668), Expect = 2e-74
 Identities = 155/382 (40%), Positives = 216/382 (56%), Gaps = 43/382 (11%)

Query: 1   MARVLLEHIYKTYPGQTEPTVKDFNLDIQDKEFTVFVGPSGCGKTTTLRMIAGLEDITEG 60
           MA V    + K + G     V   +L + + EF V +GPSG GKTT LR+IAGLE  T G
Sbjct: 1   MATVETRSLTKRFDGTN--AVDGIDLAVHEAEFLVLLGPSGSGKTTLLRLIAGLEAPTSG 58

Query: 61  NLYIGDRRVNDVPPKDRDIAMVFQNYALYPHMTVYQNMAFGLKLRKVPKAEIDRRVQEAA 120
           ++ +G R V  +PP+  ++AMVFQ+YALYPH++V  N+AF L+ +++P+  I R+V  AA
Sbjct: 59  DILVGGRVVTGLPPRAHNMAMVFQSYALYPHLSVAGNIAFPLEAQRMPREAIARKVSWAA 118

Query: 121 KILDIAHLLDRKPKALSGGQRQRVALGRAIVREPQVFLMDEPLSNLDAKLRVQMRAEIRK 180
            +  I HLL RKP+ LSGG+RQRVAL RA+VREP  FL+DEPLSNLDAKLR   R E+++
Sbjct: 119 ALFGIGHLLSRKPRQLSGGERQRVALARAVVREPVAFLLDEPLSNLDAKLRTSAREELQQ 178

Query: 181 LHQRLQTTVIYVTHDQTEAMTMGDRIVVMRDGVIQQADTPQVVYSQPKNMFVAGFIGSPA 240
           L +RL TT IYVTHDQ EA+ +GDR+ ++  G + Q  TPQ VY QP + FVA FIGSP 
Sbjct: 179 LQRRLATTTIYVTHDQIEALALGDRVAILDHGRVHQLGTPQQVYEQPADTFVATFIGSPP 238

Query: 241 MNFIRGEIVQDGDAFYFRAPSISLRLPEGRYGVLKASGAIGKPVVLGVRPEDLHDEEVFM 300
           MN +      D DA                             +V G RPE     EV+ 
Sbjct: 239 MNLV------DTDA-----------------------------LVTGFRPEHFLPREVYG 263

Query: 301 TTYPDSVLQMQVEVVEHMGSE--VY--LHTSIGPNTIVARVNPRHVY--HVGSSVKLAID 354
           +          +  +E++GS+  VY  L   + P  +++R+     +    G+    A+ 
Sbjct: 264 SDEALEPFPFHITRIENLGSDRLVYGLLEPPLPPAKVISRIPCTVTFPLETGARYPFAVR 323

Query: 355 LNKIHIFDAETEESIGFAAGPA 376
              +  FD  +  S+G A+  A
Sbjct: 324 RADLRRFDPRSGASLGVASSVA 345


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: 363
Number of extensions: 17
Number of successful extensions: 2
Number of sequences better than 1.0e-02: 1
Number of HSP's gapped: 2
Number of HSP's successfully gapped: 2
Length of query: 384
Length of database: 351
Length adjustment: 30
Effective length of query: 354
Effective length of database: 321
Effective search space:   113634
Effective search space used:   113634
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