GapMind for catabolism of small carbon sources

 

Alignments for a candidate for prdF in Pseudomonas fluorescens FW300-N2C3

Align proline racemase (EC 5.1.1.4); 4-hydroxyproline epimerase (EC 5.1.1.8) (characterized)
to candidate AO356_24910 AO356_24910 hypothetical protein

Query= BRENDA::H3ZMH5
         (331 letters)



>FitnessBrowser__pseudo5_N2C3_1:AO356_24910
          Length = 342

 Score =  184 bits (468), Expect = 2e-51
 Identities = 113/335 (33%), Positives = 183/335 (54%), Gaps = 5/335 (1%)

Query: 1   MFADHVFHVVDTHTEGEPTRIVLSGVNVKGEDIIEKREYFKEHYDWIRTALLHEPRGHSD 60
           M +  + HVV  H EGE   +++ GV       + ++  +      +R  +L+EPRG   
Sbjct: 1   MRSSKIIHVVSCHAEGEVGDVIVGGVAPPPGATVWEQSRWIAQDQTLRNFVLNEPRGGVF 60

Query: 61  QFGAVLVPSDI--ADFGVIYMDTSGYLDMCGHATMGVATVLVELGIIEKKEPYTTVKLET 118
           +   +LVP+    A    I M+ +    M G  ++ VATVL++ GI+   EP T + LE 
Sbjct: 61  RHVNLLVPAKDPRAQMAWIIMEPADTPPMSGSNSLCVATVLLDSGILPMTEPQTRLVLEA 120

Query: 119 PAGLVEAKAKVKGGVVKEVTVVDVPSFYVG-EFVIEYPGRGKIKVDVAFGGNFYVIADAR 177
           P GL+EA A  + G V+ + + +VPSF    +  IE  G G ++VD A+GG+ +VI DA+
Sbjct: 121 PGGLIEAVADCRDGKVRRIEIKNVPSFADRLDAWIEVEGLGSLQVDTAYGGDSFVIVDAQ 180

Query: 178 DLGLRVRREYIKELIPTALKLIKVANEQIKVQHPRKGVQNRINLAMLTDEPERED--SDG 235
            LG  +R +   EL+   LK+ + ANEQ+   HP     + I+   +     +E+  + G
Sbjct: 181 RLGFAIRPDEAAELVAVGLKITRAANEQLGFVHPLNPDWSHISFCQIAAPIVQENGIATG 240

Query: 236 KNVVIWGEGSVDRSPCGTGSASRVATLYSKGILKEGDIFVHESILGTQFRIKIVGTTKIG 295
            N V+   G +DRSP GTG ++R+A L++KG+++ G+ F+  SI+G++F  +I   T + 
Sbjct: 241 ANAVVIQPGKIDRSPTGTGCSARMAVLHAKGLMQVGERFIGRSIIGSEFHCRIDSLTDVA 300

Query: 296 EYTAIIPEITGSAYITKISQDIISKNDPLWKGFLL 330
              AI P I G A+IT   Q ++   DP  +G+ L
Sbjct: 301 GRPAIYPCIAGRAWITGTHQLLLDPADPWPQGYRL 335


Lambda     K      H
   0.319    0.139    0.406 

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: 267
Number of extensions: 20
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: 331
Length of database: 342
Length adjustment: 28
Effective length of query: 303
Effective length of database: 314
Effective search space:    95142
Effective search space used:    95142
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 (21.7 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