GapMind for catabolism of small carbon sources

 

Alignments for a candidate for gci in Cupriavidus basilensis 4G11

Align D-galactarolactone cycloisomerase (EC 5.5.1.27) (characterized)
to candidate RR42_RS34985 RR42_RS34985 mandelate racemase

Query= BRENDA::A9CEQ8
         (378 letters)



>FitnessBrowser__Cup4G11:RR42_RS34985
          Length = 368

 Score =  146 bits (368), Expect = 1e-39
 Identities = 118/372 (31%), Positives = 168/372 (45%), Gaps = 29/372 (7%)

Query: 1   MKITAVRTHLLEHRLD--TPFESASMRFDRRAHVLVEIECDDGTVGWGECL----GPARP 54
           M  T V+  LL+  L    P   A   F  +   +V I CDDG  G G       G +  
Sbjct: 1   MSATIVQVELLQVDLPPRVPRSDAIQSFVMQETPMVRIRCDDGAEGTGYAYTIGTGGSSV 60

Query: 55  NAAVVQAYSGWLIGQDPRQTEKIWAVLYNALRDQGQRGLSLTALSGIDIALWDIKGKHYG 114
            A +    +  LIG+DP Q E IW  L  A        ++  AL+ ID ALWD + +  G
Sbjct: 61  MALLRDHLAPRLIGRDPAQIEAIWRELLFATHATSVGAITSLALAAIDTALWDWRCRRDG 120

Query: 115 ASISMLLGGRWRESVRAYAT-GSFKRDNVDRVSDNASEMAERRAEGFHACKIKIGFG-VE 172
             + +  GG  +  V  Y T G +   + D +    SE    R  GF   K+K+G     
Sbjct: 121 QPLWLAAGGA-QPRVPVYTTEGGWLHLDADTL---VSEAVAAREAGFRGAKLKVGRARAS 176

Query: 173 EDLRVIAAVREAIGPDMRLMIDANHGYTVTEAITLGDRAAGFGIDWFEEPVVPEQLDAYA 232
           ED+  +AAVR+A+G    LM+DAN  +T  EAI      A  GI WFEEP+  + +  + 
Sbjct: 177 EDVARLAAVRDAVGDGFELMVDANQCFTAAEAIRRAPHYAELGIAWFEEPLPADDIGGHV 236

Query: 233 RVRAGQPIPVAGGETWHGRYGMWQALSAGAVDILQPDLCGCGGFSEIQKIATLATLHGVR 292
           R+ A   +P+A GE+ +      + +  GA  I+Q D+   GG +   K+A LA  H + 
Sbjct: 237 RLAASTSVPIAVGESLYSPGQFAEYVRQGACGIVQADVARIGGITPWLKVAHLAEAHNLS 296

Query: 293 IVPHVWGTGVQIAAALQFMAAMTPDPVRVNPIEPIMEFDRTHNPFRQAVLREPLEAVNGV 352
           I PH     +++  +L    A  P+   V  I  + E          A     +EA  G 
Sbjct: 297 ICPHFL---MELHVSL---CAAVPNAAWVEYIPQLDEI---------AASSVRIEA--GH 339

Query: 353 VTIPDGPGLGIE 364
              PD PGLGIE
Sbjct: 340 AIAPDAPGLGIE 351


Lambda     K      H
   0.321    0.138    0.431 

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: 415
Number of extensions: 21
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: 378
Length of database: 368
Length adjustment: 30
Effective length of query: 348
Effective length of database: 338
Effective search space:   117624
Effective search space used:   117624
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 (21.9 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 the paper from 2019 on GapMind for amino acid biosynthesis, the paper from 2022 on GapMind for carbon sources, or view the source code.

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