GapMind for catabolism of small carbon sources

 

Alignments for a candidate for lysDH in Cupriavidus basilensis 4G11

Align lysine 6-dehydrogenase (EC 1.4.1.18) (characterized)
to candidate RR42_RS18505 RR42_RS18505 saccharopine dehydrogenase

Query= BRENDA::Q3S559
         (368 letters)



>FitnessBrowser__Cup4G11:RR42_RS18505
          Length = 401

 Score =  413 bits (1062), Expect = e-120
 Identities = 220/368 (59%), Positives = 265/368 (72%), Gaps = 14/368 (3%)

Query: 3   RTQHAITVLGAGKIGFAIALLLQRTGDYAVCVADQDPSRLDAVA-ALGCQTAQIDNDAAL 61
           +T   + VLGAGKIG  IA++L  +GDY V + D++P+ L+ V   +  +          
Sbjct: 25  QTPMRVVVLGAGKIGRTIAVMLHDSGDYRVTLVDREPTHLEGVPQGIAVRVGDPGQTEDC 84

Query: 62  EAAIAGRHAVLNALPFHRAVAVAGLCARLGVHYFDLTEDVASTHAIHALGRDARAVLMPQ 121
              + G  AVLNALPFH AV VA + A LGVHYFDLTEDVA+THAI  L   AR VLMPQ
Sbjct: 85  ARLLGGAQAVLNALPFHAAVGVATVAASLGVHYFDLTEDVAATHAIRRLAEGARCVLMPQ 144

Query: 122 CGLAPGFIGIVGNDLARRF----DTLLDLRMRVGGLPRYPTNALRYNLYLEHRGADQRVL 177
           CGLAPGFIG+VGNDLA+RF      LLDL+MRVG LPRYP+NAL+YNL     G      
Sbjct: 145 CGLAPGFIGVVGNDLAQRFLRGGGELLDLKMRVGALPRYPSNALKYNLTWSTEGLINEYC 204

Query: 178 QSMRGAVDGELVKVPPMEGYETFTLDGVEYEAFNTSGGLGTLPQTLLGKARNVDYKSVRY 237
                 VDG  V+VP +EG E+F LDG+EYEAFNTSGGLGTLP+TL G+AR VDYKS+RY
Sbjct: 205 NPCEAIVDGRRVEVPALEGLESFALDGIEYEAFNTSGGLGTLPETLAGRARGVDYKSIRY 264

Query: 238 PGHCAIMKLLLNDLRLRERRELLQDILESAIPATGQDVIVILATASGY-----RGGR--L 290
           PGHCA+MKLLLNDLRLRERR+ +++I ESAIPAT QDV+++ A+A+GY     +GGR  L
Sbjct: 265 PGHCAVMKLLLNDLRLRERRDWMREIFESAIPATQQDVVIVFASATGYAASGGKGGRGPL 324

Query: 291 LQEAYSAHIHG-DTVDGHALSAIQLSTAAGICTALDLVVEGALPQRGFVGQESIPLDALL 349
            Q ++SA I G DTV GH ++AIQL+TAAGICTALDLV  G LPQ GFV QE++PLD  L
Sbjct: 325 TQASFSARIGGADTVAGH-VNAIQLTTAAGICTALDLVANGELPQAGFVAQEAMPLDVFL 383

Query: 350 ANRHGRIY 357
           ANR GR Y
Sbjct: 384 ANRFGRHY 391


Lambda     K      H
   0.323    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: 470
Number of extensions: 15
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: 368
Length of database: 401
Length adjustment: 30
Effective length of query: 338
Effective length of database: 371
Effective search space:   125398
Effective search space used:   125398
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.5 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