GapMind for catabolism of small carbon sources

 

Alignments for a candidate for antC in Cupriavidus basilensis 4G11

Align electron transfer component of the anthranilate 1,2-dioxygenase system (EC 1.14.12.1) (characterized)
to candidate RR42_RS32665 RR42_RS32665 phenol hydroxylase

Query= reanno::WCS417:GFF4631
         (335 letters)



>FitnessBrowser__Cup4G11:RR42_RS32665
          Length = 355

 Score =  161 bits (408), Expect = 2e-44
 Identities = 111/332 (33%), Positives = 162/332 (48%), Gaps = 16/332 (4%)

Query: 12  GKTLFFPVGANEILLDAALRNGIKIPLDCREGVCGTCQGRCESGDYSQDYVDEEALSSLD 71
           G+T+  P+ A + +LDA LRNG+ +P  C  G+C TC+ +   G++        AL   +
Sbjct: 10  GQTI--PIAAGQTVLDACLRNGVWLPHACCHGLCATCKVQVVEGEFEHGEASSFALMDFE 67

Query: 72  LQQRKMLSCQTRVKSDATFYFDFDSSLCNAPGPVQVKGTVSAVEQVSASTAI----LQVQ 127
               + L+C    +SD     D +    ++ G          VE  + +  I    L+V+
Sbjct: 68  RDSGQCLACCATAQSDMVIEADIEED-ADSLGLPLADYRAEVVEARALTPTIRGIWLRVK 126

Query: 128 LDQALDFLPGQYARLSVPGTDSWRSYSFANLPGNHL-QFLVRLLPDGVMSNYLRERCQVG 186
              A  F  GQY  L VPG D  R++S AN PG+ L +  VR +  G  + YL +R  VG
Sbjct: 127 GGAAAAFQAGQYLNLHVPGCDQPRAFSLANRPGDDLVELHVRRVEGGQATGYLHDRLSVG 186

Query: 187 DELLMEAPLGAFYLRHVTQ-PLVLVAGGTGLSALLGMLDQLAANGCEQPVHLYYGVRGAE 245
           DEL   AP G F++R   Q P++ +AGG+GLS+   M+  + A G   P+ L  G R   
Sbjct: 187 DELGFSAPYGRFFVRKSAQKPMLFLAGGSGLSSPRAMILDMLAAGETLPITLVQGARNRT 246

Query: 246 DLCEAARIRAYAAKIPNLRYTEVLS-APSEE-WSGKRGYLTEHFDLAELRDGSADM---- 299
           +L      RA A   PN RY   LS  P++  W G RGY+ +          +AD     
Sbjct: 247 ELYYDEAFRALAGAHPNFRYVPALSDVPADSGWDGARGYVHDVLHGLYADGATADFRGHK 306

Query: 300 -YLCGPPPMVESIQQWLADQALDGVQLYYEKF 330
            YLCGPPPM+E+  + L    L    ++ EKF
Sbjct: 307 AYLCGPPPMIEACIRTLMQGRLFEEDIHTEKF 338


Lambda     K      H
   0.320    0.136    0.412 

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: 276
Number of extensions: 22
Number of successful extensions: 6
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: 335
Length of database: 355
Length adjustment: 29
Effective length of query: 306
Effective length of database: 326
Effective search space:    99756
Effective search space used:    99756
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