GapMind for catabolism of small carbon sources

 

Alignments for a candidate for nbaD in Cupriavidus basilensis 4G11

Align 2-amino-3-carboxymuconate 6-semialdehyde decarboxylase (EC 4.1.1.45) (characterized)
to candidate RR42_RS05075 RR42_RS05075 aminocarboxymuconate-semialdehyde decarboxylase

Query= metacyc::MONOMER-13360
         (334 letters)



>FitnessBrowser__Cup4G11:RR42_RS05075
          Length = 337

 Score =  488 bits (1257), Expect = e-143
 Identities = 229/327 (70%), Positives = 268/327 (81%), Gaps = 1/327 (0%)

Query: 6   IDMHSHFFPRISEQEAAKFDANHAPWLQVSAKGDTGSIMMGKNNFRPVYQALWDPAFRIE 65
           +D+HSHFFP IS +EAA  D   APWLQ +   DT  IM G   FRPVY ALWDPA RIE
Sbjct: 7   VDIHSHFFPPISRREAAALDPVAAPWLQANGT-DTAMIMTGDQPFRPVYSALWDPARRIE 65

Query: 66  EMDAQGVDVQVTCATPVMFGYTWEANKAAQWAERMNDFALEFAAHNPQRIKVLAQVPLQD 125
           EMD  GVD+Q+ CATPVMFGY + A+ A  W++RMND+ALE  AH P R+K LAQVPLQD
Sbjct: 66  EMDRCGVDIQLMCATPVMFGYRYPAHVAVPWSQRMNDYALELCAHRPARLKALAQVPLQD 125

Query: 126 LDLACKEASRAVAAGHLGIQIGNHLGDKDLDDATLEAFLTHCANEDIPILVHPWDMMGGQ 185
           +D AC+EASRA A GH+G+QIGNHLG++DLDD  L  FL HCANE I +LVHPWDMMG  
Sbjct: 126 IDAACREASRAKAGGHVGVQIGNHLGERDLDDEGLITFLIHCANEGIAVLVHPWDMMGAP 185

Query: 186 RMKKWMLPWLVAMPAETQLAILSLILSGAFERIPKSLKICFGHGGGSFAFLLGRVDNAWR 245
           RMKKWMLPWLV+MPAETQL ILSLILSGAFERIP SLK+CF HGGGSFAFLLGR+DNAWR
Sbjct: 186 RMKKWMLPWLVSMPAETQLGILSLILSGAFERIPASLKLCFAHGGGSFAFLLGRIDNAWR 245

Query: 246 HRDIVREDCPRPPSEYVDRFFVDSAVFNPGALELLVSVMGEDRVMLGSDYPFPLGEQKIG 305
           HRDIVREDCP PPS YV+RFFVDSAVF+P AL+LLV VMGEDRVMLGSDYP+PLGEQ++G
Sbjct: 246 HRDIVREDCPHPPSSYVNRFFVDSAVFDPRALKLLVDVMGEDRVMLGSDYPYPLGEQQVG 305

Query: 306 GLVLSSNLGESAKDKIISGNASKFFNI 332
            L+ +++L ++A+ K++  NA+ FF +
Sbjct: 306 ALIRATDLADAARRKLLGANAAAFFGL 332


Lambda     K      H
   0.322    0.137    0.430 

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: 468
Number of extensions: 12
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: 334
Length of database: 337
Length adjustment: 28
Effective length of query: 306
Effective length of database: 309
Effective search space:    94554
Effective search space used:    94554
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: 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