GapMind for catabolism of small carbon sources

 

Alignments for a candidate for galE in Nitratifractor salsuginis DSM 16511

Align UDP-glucose 4-epimerase; Galactowaldenase; UDP-galactose 4-epimerase; EC 5.1.3.2 (characterized)
to candidate WP_013554916.1 NITSA_RS10015 polysaccharide biosynthesis protein

Query= SwissProt::Q9ZDJ5
         (341 letters)



>NCBI__GCF_000186245.1:WP_013554916.1
          Length = 597

 Score =  139 bits (351), Expect = 1e-37
 Identities = 109/328 (33%), Positives = 164/328 (50%), Gaps = 29/328 (8%)

Query: 5   KTLMITGGTGSFGNAVLSRFL----KSNIINDIKEIRIFSRDEKKQEDMRIALNNSKLKF 60
           K ++ITG  GS G+ +  + L    K  I+ +  E  ++   E+ ++D  +    S L  
Sbjct: 280 KRILITGAGGSIGSEICRQCLAYGAKRLILVENSEYNLYRISEELEKDRIVPRLVSVL-- 337

Query: 61  YIGDVRNYQSIDDAMHGVDYVFHAAALKQVPTCEFYPMEAINTNVLGAENVLSAAINNKV 120
              D    + +  A H  D V HAAA K VP CE  P  AI  N+LGA NV+  +I   V
Sbjct: 338 ---DRERLEEVFKAEHP-DVVIHAAAFKHVPLCELNPDTAIENNILGAMNVIDLSIRYGV 393

Query: 121 TKVIVLSTDKAVYPINAMGLSKALMEKLAIAKARMRSPGETILCVTRYGNVMASRGSVIP 180
            KV+ +S+DKAV P N MG +K ++E  A      R    T +   R+GNV+ S GSV+P
Sbjct: 394 EKVVNISSDKAVRPTNVMGATKRIIELYAQNVPNDR----TEIVSVRFGNVLGSSGSVVP 449

Query: 181 LFIHQIKQGKELTITEPSMTRFLMSLVDSVDLVLYAFEHGRQGDIFV--QKSPASTIEVL 238
            F  QI+ G  +T+T P MTR+ M + ++  LVL A    + G++F+     P   ++ L
Sbjct: 450 KFKAQIEAGGPVTVTHPEMTRYFMLIPEACQLVLQAAAMAQGGELFILDMGEPVKIVD-L 508

Query: 239 AKALQEIFGSKNAIRFI--GTRHGEKHYESLVSSEDMAKADDLGGYYRIPMDGRDLNYAK 296
           A+ +  ++G +  +  +  G R GEK YE L+ ++   K      Y  I + GR  NY  
Sbjct: 509 ARKMIRLYGKEGEVDIVYTGLRPGEKLYEELLINDAECKT----RYESIYVAGRS-NYPI 563

Query: 297 YFVTGEKKVALLDDYTSHNTKRLNLKEV 324
                EK  A +        KR+ LKE+
Sbjct: 564 -----EKLRADIRHLLEAKDKRVLLKEI 586


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: 400
Number of extensions: 16
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: 597
Length adjustment: 33
Effective length of query: 308
Effective length of database: 564
Effective search space:   173712
Effective search space used:   173712
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: 51 (24.3 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