GapMind for catabolism of small carbon sources

 

Alignments for a candidate for davT in Pedobacter sp. GW460-11-11-14-LB5

Align 5-aminovalerate transaminase (EC 2.6.1.48) (characterized)
to candidate CA265_RS18530 CA265_RS18530 aspartate aminotransferase family protein

Query= BRENDA::Q9I6M4
         (426 letters)



>FitnessBrowser__Pedo557:CA265_RS18530
          Length = 382

 Score =  204 bits (520), Expect = 3e-57
 Identities = 129/342 (37%), Positives = 199/342 (58%), Gaps = 30/342 (8%)

Query: 23  IHPVVAERAENSTVWDVEGREYIDFAGGIAVLNTGHLHPKVIAAVQEQLGKLSHTCFQVL 82
           ++ +   +A  S VWD   ++Y+D  GG AV++ GH +P  +  + +QL K+      V 
Sbjct: 9   LNDIEITKAAGSNVWDANDQQYLDLYGGHAVISIGHTNPHYVNRLTDQLNKVGFYSNSV- 67

Query: 83  AYEPYIELAEEIAKRVPGDFPKKTLLVTSGSEAVENAVKIARAATGRAGVIAFTGAYHGR 142
                ++LAE++ + V G    +  L  SG+EA ENA+K+A    GR  VIAFTGA+HGR
Sbjct: 68  KIPLQVQLAEKLGE-VSGKKDFQLFLCNSGAEANENALKLASFYNGRKKVIAFTGAFHGR 126

Query: 143 TMMTLGLTG--KVVPYSAGMGLMPGGIFRALAPCELHGVSEDDSIASIERIFKNDAQPQD 200
           T + + +T   K+V   A +      IF              ++  ++E  FK  AQ  +
Sbjct: 127 TSLAVAVTDNPKIV---APVNQTENVIFLPF-----------NNEIALEETFK--AQGNE 170

Query: 201 IAAIIIEPVQGEGGFYVNSKSFMQRLRALCDQHGILLIADEVQTGAGRTGTFFATEQLGI 260
           I+A+IIE +QG GG    SKSF+Q++R+LCD++  + IAD VQ G GRTG+F++ +  G+
Sbjct: 171 ISAVIIEGIQGVGGIKEASKSFLQKIRSLCDEYNAVYIADSVQCGYGRTGSFYSHDYSGV 230

Query: 261 VPDLTTFAKSVGGGFPISGVAGKAEIMDAIAP--GGLGGTYAGSPIACAAALAVLKVFEE 318
             D+ T AK +G GFP++G++    I     P  G LG T+ G+ +ACAAALAVL+V E+
Sbjct: 231 EADVYTMAKGMGNGFPVAGIS----IASKFKPWHGELGTTFGGNHLACAAALAVLEVMEK 286

Query: 319 EKLLERSQAVGERLKAGLREIQAKHKVIGDVRGLGSMVAIEL 360
           + L++ ++ VG  L A L+    K + + +VRG G M+ IEL
Sbjct: 287 DNLIKNAEEVGNYLIAELK----KFEQVVEVRGRGLMIGIEL 324


Lambda     K      H
   0.319    0.137    0.393 

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: 384
Number of extensions: 24
Number of successful extensions: 5
Number of sequences better than 1.0e-02: 1
Number of HSP's gapped: 2
Number of HSP's successfully gapped: 1
Length of query: 426
Length of database: 382
Length adjustment: 31
Effective length of query: 395
Effective length of database: 351
Effective search space:   138645
Effective search space used:   138645
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: 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