GapMind for catabolism of small carbon sources

 

Alignments for a candidate for manA in Aquimarina macrocephali JAMB N27

Align mannose-6-phosphate isomerase (EC 5.3.1.8) (characterized)
to candidate WP_035091175.1 Z054_RS0109375 class I mannose-6-phosphate isomerase

Query= BRENDA::Q9AGZ4
         (315 letters)



>NCBI__GCF_000520995.1:WP_035091175.1
          Length = 322

 Score =  188 bits (478), Expect = 1e-52
 Identities = 117/322 (36%), Positives = 171/322 (53%), Gaps = 25/322 (7%)

Query: 1   MTHPLFLEPVFKERLWGGTKLRDAFGYAIPSQKTGECWAVSAHANGPSAVKNGPLAGKTL 60
           M +PL   P+ KE++WGG KL+     +  +   GE W +S      S V NG L GK L
Sbjct: 1   MLYPLKFNPILKEKIWGGNKLKTILNKSTSNTNVGESWEISTVDKDISIVANGELYGKKL 60

Query: 61  DQVWQDHP-EIFG------FPDRKVFPLLVKLLDANMDLSVQVHPDDDYAKLHENGDLGK 113
           D++ ++H  E+ G      F D+  FPLL+K +DA  DLSVQ+HP+D+ AK   +   GK
Sbjct: 61  DELIREHKAELLGKKVYQEFGDQ--FPLLLKFIDAKEDLSVQLHPNDELAKKRHDS-FGK 117

Query: 114 TECWYIIDCKDDAELILGHHAST-KEEFKQRIESGDWNGLLRRIKIKPGDFFYVPSGTLH 172
           TE WY++    DA+LI+G + +T KEE++  +E G    LL    I  GD +++ +G +H
Sbjct: 118 TEMWYVVQADVDAKLIVGFNKNTSKEEYQTYLEEGKITKLLNFEDISKGDSYFIKTGKIH 177

Query: 173 ALCEGTLVLEIQQNSDTTYRVYDYDRCNDQGQKRTLHIEKAMEVITIPHID--KVHTPEV 230
           A+  G L+ EIQQ SD TYRVYD+DR +D G  R LH + A++ +     D  K+     
Sbjct: 178 AIGRGVLIAEIQQTSDITYRVYDWDRKDDTGNSRELHTDLALDALDYNTKDDFKLIYNRK 237

Query: 231 KEVGNAEITVYVQSDYFSVYKWKISGRA-----AFPSYQTYLLGSVLSGSGRIINNGSQY 285
           K   N         +YF+    KI  R      A  S++ Y+    L G+G I+ N    
Sbjct: 238 KNTANE----VADCNYFTTNYLKIEQRLDRVYNAIDSFKIYM---CLEGTGNIMCNTHSE 290

Query: 286 ECNAGSHFVLPAHFGEFSIEGT 307
               G   ++PA F +  I+GT
Sbjct: 291 SIGKGETILIPAMFDKIEIKGT 312


Lambda     K      H
   0.319    0.138    0.435 

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: 329
Number of extensions: 25
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: 315
Length of database: 322
Length adjustment: 27
Effective length of query: 288
Effective length of database: 295
Effective search space:    84960
Effective search space used:    84960
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 (21.8 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