GapMind for catabolism of small carbon sources

 

Alignments for a candidate for galE in Rhodomicrobium vannielii ATCC 17100

Align UDP-glucose 4-epimerase; UDP-galactose 4-epimerase; Uridine diphosphate galactose 4-epimerase; EC 5.1.3.2 (characterized)
to candidate WP_013421188.1 RVAN_RS18385 NAD-dependent epimerase/dehydratase family protein

Query= SwissProt::A0R5C5
         (313 letters)



>NCBI__GCF_000166055.1:WP_013421188.1
          Length = 318

 Score =  154 bits (390), Expect = 2e-42
 Identities = 103/314 (32%), Positives = 148/314 (47%), Gaps = 15/314 (4%)

Query: 2   RTLVTGAAGFIGSTLVDRLLADGHGVVGLDDLSSGRAENLHSAENSDKFEFVKADIVDAD 61
           R LVTG AGF+GS L+DRLLADGH V+ +D+L +G   N+       +FEF++ D+    
Sbjct: 10  RVLVTGGAGFLGSHLIDRLLADGHEVLCVDNLFTGTKRNIDHLHGQPRFEFMRHDVT--- 66

Query: 62  LTGLLAEFKPEVIFHLAAQISVKRSVDDPPFDATVNVVGTVRLAEAARLAGVRKVVHTSS 121
              L    + + I++LA   S      DP      +V G + +   A+    R  +  +S
Sbjct: 67  ---LPLYVEVDEIYNLACPASPVHYQHDPVQTTKTSVHGAINMLGLAKRLKCR--ILQAS 121

Query: 122 GGSVYGTPPAYPTSEDM-----PVNPASPYAAGKVAGEVYLNMYRNLYDLDCSHIAPANV 176
              VYG P  +P  ED      P+ P S Y  GK   E     Y   + LD       N 
Sbjct: 122 TSEVYGDPAVHPQREDYWGNVNPIGPRSCYDEGKRCAETLFFDYNRQHQLDIKVARIFNT 181

Query: 177 YGPRQDPHGEAGVVAIFSEALLAGRTTKIFGDGSDTRDYVFVDDVVDAFVR-AGGPAGGG 235
           YGPR     +  VV+ F    L      ++GDG  TR + +VDD++D  VR    PAG  
Sbjct: 182 YGPRMH-RADGRVVSNFIVQALTNEPITLYGDGRQTRSFCYVDDLIDGLVRLMNSPAGFI 240

Query: 236 QRFNVGTGVETSTRELHTAIAGAVGAPDEPEFHPPRLGDLRRSRLDNTRAREVLGWQPQV 295
              N+G   E S  EL   +     +  E  + P    D ++ + D   A+  LGWQP+V
Sbjct: 241 GPVNLGNPGEFSMLELAREVVRQTDSASEIVYRPLPADDPKQRQPDIALAQAKLGWQPEV 300

Query: 296 ALAEGIAKTVEFFR 309
            L+EG+  T+ +FR
Sbjct: 301 PLSEGLKPTIAYFR 314


Lambda     K      H
   0.317    0.136    0.396 

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: 283
Number of extensions: 19
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: 313
Length of database: 318
Length adjustment: 27
Effective length of query: 286
Effective length of database: 291
Effective search space:    83226
Effective search space used:    83226
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.3 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 41 (21.6 bits)
S2: 48 (23.1 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