GapMind for catabolism of small carbon sources

 

Alignments for a candidate for galE in Cronobacter universalis NCTC 9529

Align UDP-glucose 4-epimerase; EC 5.1.3.2; Galactowaldenase; UDP-galactose 4-epimerase (uncharacterized)
to candidate WP_007699418.1 AFK65_RS12810 UDP-N-acetylglucosamine 4,6-dehydratase/5-epimerase

Query= curated2:A8GWP0
         (341 letters)



>NCBI__GCF_001277175.1:WP_007699418.1
          Length = 344

 Score =  434 bits (1116), Expect = e-126
 Identities = 218/336 (64%), Positives = 276/336 (82%), Gaps = 5/336 (1%)

Query: 1   MFVDKTLLITGGTGSFGNAVLSRFLKNDIIKDIKEIRIFSRDEKKQEDMRIALNNPKIKF 60
           MF +K LLITGGTGSFGNAVL+RFL  DI    KEIRIFSRDEKKQ+DMR   NN K+KF
Sbjct: 1   MFKNKVLLITGGTGSFGNAVLNRFLNTDI----KEIRIFSRDEKKQDDMRKKYNNNKLKF 56

Query: 61  YIGDVRNYNSIDDAMKDVDYVFHAAALKQVPTCEFYPMEAINTNILGAENVLRAATINKV 120
           YIGDVR+Y SI +A + VD+++HAAALKQVP+CEF+PMEA+ TN+LG ENVL AA  N+V
Sbjct: 57  YIGDVRDYGSILNATRGVDFIYHAAALKQVPSCEFHPMEAVKTNVLGTENVLEAAIANEV 116

Query: 121 AKVIVLSTDKAVYPINAMGLSKALMEKLAIAKARMNVRDKTVFCVTRYGNVMASRGSVIP 180
            +V+ LSTDKAVYPINAMG+SKA+MEK+ +AK+R    +KTV C TRYGNVMASRGSVIP
Sbjct: 117 KRVVCLSTDKAVYPINAMGISKAMMEKVMVAKSRNVDTNKTVICGTRYGNVMASRGSVIP 176

Query: 181 LFINQIKQNKDLTITEPSMTRFLMSLVDSVDLVLYAFEYGHQGDIFVQKSPASTIEVLAK 240
           LF++ IK ++ LTIT+P+MTRF+M+L D+VDLVLYAFE+G+ GDIFVQK+PA+TIE LA 
Sbjct: 177 LFVDLIKADQPLTITDPNMTRFMMTLEDAVDLVLYAFEHGNNGDIFVQKAPAATIETLAI 236

Query: 241 ALQGIFNSK-NKIRFIGTRHGEKHYESLVSSEEMAKAEDLGNYYRIPMDGRDLNYAKYFV 299
           AL+ + N + + I  IGTRHGEK YE+L+S EEM  A D+G+YYR+P D RDLNY KY  
Sbjct: 237 ALKELLNKEHHPINIIGTRHGEKLYEALLSREEMIAAVDMGDYYRVPPDLRDLNYGKYVE 296

Query: 300 EGEKKIALLEDYTSHNTKRLNLEEVKELLLNLDYVQ 335
           +G+++I+ +EDY SHNT RL++E +K+LLL L +++
Sbjct: 297 QGDRRISEVEDYNSHNTTRLDVEGMKKLLLKLSFIR 332


Lambda     K      H
   0.319    0.135    0.373 

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: 398
Number of extensions: 19
Number of successful extensions: 3
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: 341
Length of database: 344
Length adjustment: 29
Effective length of query: 312
Effective length of database: 315
Effective search space:    98280
Effective search space used:    98280
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