GapMind for catabolism of small carbon sources

 

Alignments for a candidate for galT in Flavobacterium beibuense F44-8

Align UTP--hexose-1-phosphate uridylyltransferase (EC 2.7.7.10) (characterized)
to candidate WP_035135395.1 Q763_RS14005 UDP-glucose--hexose-1-phosphate uridylyltransferase

Query= reanno::Cola:Echvi_0695
         (347 letters)



>NCBI__GCF_000769915.1:WP_035135395.1
          Length = 340

 Score =  455 bits (1171), Expect = e-133
 Identities = 208/337 (61%), Positives = 258/337 (76%)

Query: 3   DFNFEDHSHRRYNPFTGDWLQVSPHRGKRPWQGQEEDTAEAQKPAYDEKCYLCPGNTRIN 62
           D N  ++ HRRYN  TG+W+ VSPHR KRPWQGQ E  +   +P YD  CYLCPGN+R  
Sbjct: 2   DKNLNEYPHRRYNALTGEWVLVSPHRSKRPWQGQVEKHSAEVRPQYDPGCYLCPGNSRSG 61

Query: 63  GEKNPDYTGAYVFQNDFGALTSDIPQGEMSEGEFFRAKSERGICKVICFSPRHDLTIPEL 122
           GE+NPDY   YVF NDF AL  D P  ++ E + F+A+SE+GIC+VICFSP H LTIP++
Sbjct: 62  GEQNPDYKDVYVFINDFSALLKDSPDFDVVEDDIFKAESEKGICRVICFSPDHSLTIPQM 121

Query: 123 DVQAITKVVELWKKEYQELGGKDFINHVQIFENKGSVMGCSNPHPHGQIWAQESIPVEPA 182
            V+ I KVV+LW +EY  LG    IN+VQIFENKG +MGCSNPHPHGQIWA + +PVEP+
Sbjct: 122 KVEDIRKVVDLWIEEYHTLGSDPEINYVQIFENKGEIMGCSNPHPHGQIWASQKLPVEPS 181

Query: 183 KKQVKFGEYYQKYGRSMVLDYVYEELKKGERILFENDYFVGLVPFWAVWPFEAMIAPKTH 242
           KKQ    EY+QK+G +++ DY+ +EL+K ERI+FEN++F  +VPFWA WP+EAMI PK  
Sbjct: 182 KKQHYQLEYFQKHGDTLLSDYLQKELQKDERIIFENNHFAAIVPFWATWPYEAMIIPKRA 241

Query: 243 IASLSEMDAAQMEALADAYRQLAIMYDNVFKVSFPYSAGIHQAPTDGQNHPEWDLHMVFY 302
           +A +++M   +  ALAD Y++L ++YD VF VSFPYSAGIHQAPTDG+ H EW  HM FY
Sbjct: 242 MARITDMTDDEKTALADTYKRLTMIYDKVFDVSFPYSAGIHQAPTDGKEHNEWHWHMAFY 301

Query: 303 PPLLRSATVKKFMVGYEMLANPQRDITAESAVKILKS 339
           PPLLRSATVKKFMVGYEMLA PQRDIT ESA +ILK+
Sbjct: 302 PPLLRSATVKKFMVGYEMLATPQRDITPESAAQILKN 338


Lambda     K      H
   0.319    0.136    0.425 

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: 464
Number of extensions: 18
Number of successful extensions: 1
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: 347
Length of database: 340
Length adjustment: 29
Effective length of query: 318
Effective length of database: 311
Effective search space:    98898
Effective search space used:    98898
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 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