GapMind for catabolism of small carbon sources

 

Alignments for a candidate for manA in Mucilaginibacter mallensis MP1X4

Align Mannose-6-phosphate isomerase; EC 5.3.1.8; Phosphohexomutase; Phosphomannose isomerase; PMI (uncharacterized)
to candidate WP_091369970.1 BLU33_RS05090 mannose-6-phosphate isomerase

Query= curated2:Q59935
         (316 letters)



>NCBI__GCF_900105165.1:WP_091369970.1
          Length = 326

 Score =  190 bits (483), Expect = 3e-53
 Identities = 118/306 (38%), Positives = 170/306 (55%), Gaps = 16/306 (5%)

Query: 4   PLFLQSQMHKKIWGGNR----LRKEFGYDIPSETTGEYWAISAHPNGVSVVKNGVYKGVP 59
           PL  ++    KIWGG +    L K+FG D+P+   GE W IS   + VSVV+NG   G  
Sbjct: 6   PLKFKTIFKDKIWGGQKINTYLHKDFG-DLPN--CGETWEISGVKSDVSVVENGSLIGES 62

Query: 60  LDELYAEHRELFGNSK-----SSVFPLLTKILDANDWLSVQVHPDNAYALEHEGELGKTE 114
           L +L  ++++     K      ++FPLL K +DAN+ LS+QVHPD+  A E     GKTE
Sbjct: 63  LADLLEQYKDELVGKKVYDHFGNIFPLLVKFIDANEDLSIQVHPDDKLAKERHNSFGKTE 122

Query: 115 CWYVISADEGAEIIYGHEAK-SKEELRQMIAAGDWDHLLTKIPVKAGDFFYVPSGTMHAI 173
            WYVI AD G+ +I G   + ++ E  +   +G    +L K  VKAGD F++P+G +H I
Sbjct: 123 MWYVIEADPGSTLIAGFNKELTQAEYLEKFNSGHLTDVLNKEDVKAGDVFFLPAGRVHTI 182

Query: 174 GKGIMILETQQSSDTTYRVYDFDRKDDQGRKRALHIEQSIDVLTIGKPANATPAWLSLQG 233
           GKG++I E QQ+SD TYR+YDFDR DD+G KR LH E+++  +           +   + 
Sbjct: 183 GKGLLIAEIQQTSDITYRIYDFDRVDDKGNKRELHTEEALAAIDYKHYPEYKTLYTPAKD 242

Query: 234 LETTVLVSSPFFTVYKWQISGS-VKMQQTAPYLLVSV-LAGQGRITVGLEQYALRKGDHL 291
            ET  LVS P+FT      + S VK   +    ++ V L G   I    E Y ++ G+ +
Sbjct: 243 -ETVHLVSCPYFTTNLLDFNESTVKDYSSLDSFVIHVCLEGSYEIKYNGETYPVKMGECI 301

Query: 292 ILPNTI 297
           +LP  I
Sbjct: 302 LLPKVI 307


Lambda     K      H
   0.317    0.135    0.408 

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: 292
Number of extensions: 21
Number of successful extensions: 4
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: 316
Length of database: 326
Length adjustment: 28
Effective length of query: 288
Effective length of database: 298
Effective search space:    85824
Effective search space used:    85824
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.

Links

Downloads

Related tools

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