GapMind for catabolism of small carbon sources

 

Alignments for a candidate for galE in Pseudomonas stutzeri A1501

Align UDP-glucose 4-epimerase (EC 5.1.3.2) (characterized)
to candidate WP_041755184.1 PST_RS00435 dTDP-glucose 4,6-dehydratase

Query= BRENDA::P9WN67
         (314 letters)



>NCBI__GCF_000013785.1:WP_041755184.1
          Length = 356

 Score =  144 bits (364), Expect = 2e-39
 Identities = 111/337 (32%), Positives = 164/337 (48%), Gaps = 36/337 (10%)

Query: 1   MRALVTGAAGFIGSTLVDRLLADG-HSVVGLDNFATGRATNLEHLAD---NSAHVFVEAD 56
           MR LVTG AGFIGS L+  L+ D  HSV+ LD      A NLE LA    N  + F++AD
Sbjct: 1   MRILVTGGAGFIGSALIRHLILDTEHSVLNLDKLTY--AGNLESLASVEGNPRYQFLQAD 58

Query: 57  IVTAD-LHAILEQHRPEVVFHLAAQIDVRRSVADPQFDAAVNVIGTVRLAEAAR------ 109
           I   + +   L   +P+ + HLAA+  V RS+  P      N++GT +L EAAR      
Sbjct: 59  IADRERVSEALLDFQPDAIMHLAAESHVDRSIDGPAEFIQTNIVGTYQLLEAARAYWQTL 118

Query: 110 ---QTGVRKIVHTSSG---GSIYGTPPEYPTPETAPTDPASPYAAGKVAGEIYLNTFRHL 163
              +    +  H S+    G ++G    +   ET P  P+SPY+A K + +  +  ++  
Sbjct: 119 PAERRAAFRFHHISTDEVYGDLHGVDDLFT--ETTPYAPSSPYSASKASSDHLVRAWQRT 176

Query: 164 YGLDCSHIAPANVYGPRQDPHGEAGVVAIFAQALLSGKPTRVFGDGTNTRDYVFVDDVVD 223
           YGL       +N YGP   P     +V + A   L GKP  V+GDG+  RD++FV+D   
Sbjct: 177 YGLPVLITNCSNNYGPFHFPEKLIPLVILNA---LDGKPLPVYGDGSQIRDWLFVEDHAR 233

Query: 224 AFVRVSADVGGGLRFNIGTGKETSDRQLHSAVAAAVG--GPDDP----------EFHPPR 271
           A  +V ++   G  +NIG   E  + ++   + A +    P+ P           F   R
Sbjct: 234 ALFKVVSEGKVGETYNIGGHNEQKNIEVVRGICALLEELAPNKPAGLARYEDLITFVKDR 293

Query: 272 LGDLKRSCLDIGLAERVLGWRPQIELADGVRRTVEYF 308
            G   R  +D    ER LGW PQ     G+R+TV+++
Sbjct: 294 PGHDLRYAIDASKIERELGWVPQETFQSGLRKTVQWY 330


Lambda     K      H
   0.320    0.137    0.410 

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: 262
Number of extensions: 13
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: 314
Length of database: 356
Length adjustment: 28
Effective length of query: 286
Effective length of database: 328
Effective search space:    93808
Effective search space used:    93808
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 24 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