GapMind for catabolism of small carbon sources

 

Alignments for a candidate for manA in Mucilaginibacter mallensis MP1X4

Align Mannose-6-phosphate isomerase ManA; Phosphohexomutase; Phosphomannose isomerase; PMI; EC 5.3.1.8 (characterized)
to candidate WP_091370770.1 BLU33_RS07230 mannose-6-phosphate isomerase

Query= SwissProt::O31646
         (315 letters)



>NCBI__GCF_900105165.1:WP_091370770.1
          Length = 329

 Score =  167 bits (423), Expect = 3e-46
 Identities = 107/308 (34%), Positives = 165/308 (53%), Gaps = 10/308 (3%)

Query: 1   MTTEPLFFKPVFKERIWGGTALADF-GYTIPSQRTGECWAFAAHQNGQSVVQNGMYKGFT 59
           +T  PL FKP+++ R+WGG  LA      +P    GE W  +   +  SVV NG+Y+G+T
Sbjct: 4   ITLHPLLFKPIYQYRLWGGRRLAGLLKEPLPQGPVGEAWILSDRDDHASVVTNGLYQGYT 63

Query: 60  LSELW-EHHRHLFGQLEG--DRFPLLTKILDADQDLSVQVHPNDEYANIHENGELGKTEC 116
           L++L+ ++  ++ G+L    DRFPLL K LD  + LS+QVHP+D+       G+ GKTE 
Sbjct: 64  LTQLFAQYPENIMGKLASTFDRFPLLLKFLDCKEVLSIQVHPSDDQKEYIPPGDTGKTEA 123

Query: 117 WYIIDCQKDAEIIYG-HNATTKEELTTMIERGEWDELLRRVKVKPGDFFYVPSGTVHAIG 175
           W +++  K A +  G    T  E+L   +   +  + +     K GD  ++ SGTVH + 
Sbjct: 124 WVVLETGKKALVYSGLKPGTNAEDLRKALAVHKVADYIHNFTPKDGDAVFIHSGTVHTLA 183

Query: 176 KGILALETQQNSDTTYRLYDYDRKDAE-GKLRELHLKKSIEVIEVPSIPERHTVHH--EQ 232
             ++  E Q+NSDTTYRLYD+DR DA+ GK REL + K+I  I+  +I +   V    E 
Sbjct: 184 -DVVVFEVQENSDTTYRLYDWDRVDAKTGKPRELDVDKAIACIDF-NITDVEPVKPKIES 241

Query: 233 IEDLLTTTLIECAYFSVGKWNLSGSASLKQQKPFLLISVIEGEGRMISGEYVYPFKKGDH 292
              +L   L    +F + +       S+  +    ++  ++GEG +      Y   KGD 
Sbjct: 242 ALPILREQLFNNEHFILWRIQTEDQFSVGAEDVPRILVCVDGEGAVHYDGTDYLITKGDV 301

Query: 293 MLLPYGLG 300
           ML+P  LG
Sbjct: 302 MLIPAVLG 309


Lambda     K      H
   0.319    0.138    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: 319
Number of extensions: 18
Number of successful extensions: 6
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: 315
Length of database: 329
Length adjustment: 28
Effective length of query: 287
Effective length of database: 301
Effective search space:    86387
Effective search space used:    86387
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: 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