GapMind for catabolism of small carbon sources

 

Alignments for a candidate for manA in Fibrella aestuarina BUZ 2

Align Mannose-6-phosphate isomerase; EC 5.3.1.8; Phosphohexomutase; Phosphomannose isomerase; PMI (uncharacterized)
to candidate WP_015332587.1 FAES_RS17615 mannose-6-phosphate isomerase class I

Query= curated2:Q59935
         (316 letters)



>NCBI__GCF_000331105.1:WP_015332587.1
          Length = 331

 Score =  179 bits (453), Expect = 1e-49
 Identities = 112/319 (35%), Positives = 163/319 (51%), Gaps = 25/319 (7%)

Query: 1   MAEPLFLQSQMHKKIWGGNRLRKEFGYDIPS-------ETTGEYWAISAHPNGVSVVKNG 53
           M  PL    Q   KIWGG++++   G D P+          GE W IS  P  +SVVK G
Sbjct: 1   MLYPLTFTPQFKDKIWGGHKIKTILGKDFPTGPDGQPLPNCGETWEISGVPGNISVVKEG 60

Query: 54  VYKGVPL--------DELYAEH-RELFGNSKSSVFPLLTKILDANDWLSVQVHPDNAYAL 104
              G  L        +EL  +H  E +GN     FPLL K +DAND LS+QVHP++  A 
Sbjct: 61  ALVGENLQAILEKFKEELVGKHVYETYGNE----FPLLVKFIDANDDLSIQVHPNDELAR 116

Query: 105 EHEGELGKTECWYVISADEGAEIIYGHEAK-SKEELRQMIAAGDWDHLLTKIPVKAGDFF 163
                 GKTE WY++ ADEGA++  G   + +K+E  + +A      +L     K GD F
Sbjct: 117 ARHNSFGKTEMWYILQADEGAKLNSGFNREVTKDEYVKAVADNTLPEILNIEEAKPGDVF 176

Query: 164 YVPSGTMHAIGKGIMILETQQSSDTTYRVYDFDRKDDQGRKRALHIEQSIDVLTIGKPAN 223
           ++P+G +H IGKG+++ E QQ+SD TYR+YDFDRKDD+G+ R LH EQ++D +      +
Sbjct: 177 FLPAGRVHYIGKGLLLAEIQQTSDITYRIYDFDRKDDKGQTRELHTEQAVDAIDYHYYGD 236

Query: 224 ATPAWLSLQGLETTVLVSSPFFTVYKWQISGSVKMQQTAPYLLVSVLAGQGRITV---GL 280
              ++   +  E    V S +F          V    T     V ++   G +T+   G 
Sbjct: 237 YKTSYDHKRN-EGVNAVKSDYFVTNVLDFDQEVMHDYTHLDSFVILVCVDGSLTIQATGG 295

Query: 281 EQYALRKGDHLILPNTIKS 299
               L+KG+  ++P +  S
Sbjct: 296 YSVPLKKGECALIPASTPS 314


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: 319
Number of extensions: 28
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: 331
Length adjustment: 28
Effective length of query: 288
Effective length of database: 303
Effective search space:    87264
Effective search space used:    87264
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.

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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