GapMind for catabolism of small carbon sources

 

Alignments for a candidate for galT in Methylocystis bryophila S285

Align UTP--hexose-1-phosphate uridylyltransferase (EC 2.7.7.10) (characterized)
to candidate WP_085772480.1 B1812_RS16015 UDP-glucose--hexose-1-phosphate uridylyltransferase

Query= reanno::Pedo557:CA265_RS06120
         (351 letters)



>NCBI__GCF_002117405.1:WP_085772480.1
          Length = 344

 Score =  390 bits (1001), Expect = e-113
 Identities = 182/333 (54%), Positives = 229/333 (68%)

Query: 7   LDSNPHTRLNILTGEWVLVSPHRTKRPWQGKVEDVTPDNRPEYDPKCYLCPGNSRADGDS 66
           L + PH R N LTG W LVSPHRT+RPW+G++E    +  P   P CYLCPG  RA+G  
Sbjct: 5   LQNAPHRRFNPLTGAWALVSPHRTQRPWRGQLEASAAETLPRRQPGCYLCPGEVRANGKR 64

Query: 67  NPEYTESFVFNNDFAALLEDTPAGNMNEHDLLVASNQRGLCKVISFSPKHHLTLPEMSVK 126
           NP+Y   FVF+NDF ALL D     + E +LL+A  + G C+V+ FSP+H LTL  M  +
Sbjct: 65  NPDYETVFVFDNDFPALLPDADGKAVEEGELLIARPETGFCRVLCFSPRHDLTLSRMETR 124

Query: 127 AITAVVNVWQNEFNSLAENNWIKYIQIFENKGEIMGCSNPHPHGQIWSQGDIPLEIAKET 186
            I +VV  W++E+ +L   + ++Y+QIFEN+G +MG SNPHPH QIW+   +P E  KE 
Sbjct: 125 DIASVVEAWRDEYVALGARDNVRYVQIFENRGAMMGASNPHPHCQIWASSSLPDEPLKED 184

Query: 187 ERQKSYYAIHKRSLLSDYLKLEQKKKERIIFENDHFAVLVPFWAVWPYETMIISKRHVNS 246
           ++Q  Y A     LL DYL  E+  KERII END F VLVPFWAVWP+ETMIISKRH   
Sbjct: 185 QKQADYLARKGSCLLCDYLACERDAKERIICENDAFLVLVPFWAVWPFETMIISKRHFGG 244

Query: 247 IRLFTEAEKESLAEAIKVLTTKYDNLFETSFPYSAGMHQAPVNNGYYPEWHWHMHFYPPL 306
           +   T AE E+LA+ +K LTT+YDNLF   FPY+ G+H  P +   YP WH+H HFYPPL
Sbjct: 245 LEALTNAEVEALADVLKRLTTRYDNLFAAPFPYTMGLHPQPTDGRAYPHWHFHAHFYPPL 304

Query: 307 LRSASVKKFMVGYEMLANPQRDITPEFAANRLK 339
           LRSA+++KFMVGYEMLA PQRDITPE AA  L+
Sbjct: 305 LRSATIRKFMVGYEMLAAPQRDITPEQAAASLR 337


Lambda     K      H
   0.317    0.133    0.414 

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: 461
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: 351
Length of database: 344
Length adjustment: 29
Effective length of query: 322
Effective length of database: 315
Effective search space:   101430
Effective search space used:   101430
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 (21.7 bits)
S2: 49 (23.5 bits)

This GapMind analysis is from Apr 09 2024. 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