GapMind for catabolism of small carbon sources

 

Alignments for a candidate for manA in Arenitalea lutea P7-3-5

Align Putative mannose-6-phosphate isomerase YvyI; EC 5.3.1.8; Phosphohexomutase; Phosphomannose isomerase; PMI (uncharacterized)
to candidate WP_019386498.1 P735_RS0102870 hypothetical protein

Query= curated2:P39841
         (316 letters)



>NCBI__GCF_000283015.1:WP_019386498.1
          Length = 322

 Score =  186 bits (473), Expect = 5e-52
 Identities = 116/306 (37%), Positives = 156/306 (50%), Gaps = 18/306 (5%)

Query: 5   PIFLTPVFKEKIWGGTALRDRFGYSIPSESTGECWAISAHPKGPSTVANGPYKGKTLIEL 64
           PI  +P+ KEKIWGG  L    G     ++ GE W IS      S V NG YKG+ L EL
Sbjct: 5   PIKFSPILKEKIWGGNKLNKVLGKPSIGDNVGESWEISDVNGNVSVVNNGFYKGQNLKEL 64

Query: 65  WEEHREVFGGVE-----GDRFPLLTKLLDVKEDTSIKVHPDDYYAGENEEGELGKTECWY 119
             EH+  F G       G  FPLL K LD K D S++VHPDD  A +  +   GKTE WY
Sbjct: 65  LTEHKHNFVGKNNFENFGTNFPLLIKFLDAKTDLSVQVHPDDKMAKKYHDS-FGKTEMWY 123

Query: 120 IIDCKENAEIIYG-HTARSKTELVTMINSGDWEGLLRRIKIKPGDFYYVPSGTLHALCKG 178
           I+D   NA I+ G     +  +++  I + + E +  R ++K GD Y++P+G +HA+  G
Sbjct: 124 IMDSDANANIVLGLKDKNTNPKMLNHITAENVESIFNREQVKKGDSYFIPAGKIHAIGAG 183

Query: 179 ALVLETQQNSDATYRVYDYDRLDSNGSPRELHFAKAVNAATVPHVDGYIDESTESRKGI- 237
            L  E QQ SD TYRVYD+DR D++G  RELH   A  A          D S +S   I 
Sbjct: 184 VLAAEIQQTSDITYRVYDWDREDTHGKKRELHTKLAEKATK------QFDSSGKSNYTIN 237

Query: 238 --TIKTFVQGEYFSVYKWDINGEAEMAQD--ESFLICSVIEGSGLLKYEDKTCPLKKGDH 293
                     EYF+    DIN   E      +SF+I   +EGS  +  +  T  +  G+ 
Sbjct: 238 QDNTANLASCEYFTTNILDINSVQEKCYSHLDSFIIFMCVEGSASISVDGHTEIVNTGET 297

Query: 294 FILPAQ 299
            +LPA+
Sbjct: 298 ILLPAK 303


Lambda     K      H
   0.317    0.137    0.421 

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: 296
Number of extensions: 13
Number of successful extensions: 5
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: 322
Length adjustment: 28
Effective length of query: 288
Effective length of database: 294
Effective search space:    84672
Effective search space used:    84672
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