GapMind for catabolism of small carbon sources

 

Alignments for a candidate for manX in Streptococcus massiliensis 4401825

Align PTS system mannose-specific EIIAB component; EC 2.7.1.-; EC 2.7.1.69 (characterized)
to candidate WP_018370772.1 BN415_RS05235 PTS mannose transporter subunit IIAB

Query= CharProtDB::CH_088329
         (323 letters)



>NCBI__GCF_000341525.1:WP_018370772.1
          Length = 329

 Score =  239 bits (609), Expect = 9e-68
 Identities = 133/329 (40%), Positives = 192/329 (58%), Gaps = 13/329 (3%)

Query: 1   MTIAIVIGTHGWAAEQLLKTAEMLLGEQENVGWIDFVPGENAETLIEKYNAQLAKLDTTK 60
           M+I I+I +HG  A  + ++  M+ G+QE V  + F+P E  + L  K+N  +A  D   
Sbjct: 1   MSIGIIIASHGEFASGIHQSGSMIFGDQEKVQVVTFMPSEGPDDLYAKFNNAVAAFDADD 60

Query: 61  GVLFLVDTWGGSPFNAASRIVVDK--EHYEVIAGVNIPMLVETLMAR--DDDPSFDELVA 116
            VL L D W GSPFN ASR++ +     + +I G+N+PML++    R  D +   + + A
Sbjct: 61  EVLVLADLWSGSPFNQASRVMGENPDRKFAIITGLNLPMLIQAYTERMMDANAGVEAVAA 120

Query: 117 LAVETGREGVKALKAKPVEKAAPAPAAAAPKAAPTP--AKPMGP---NDYMVIGLARIDD 171
             ++  ++GVKAL     E+  PA   A   AAP    A P G    +  + I LARID 
Sbjct: 121 NIIKEAKDGVKALP----EELNPAEVTATNAAAPVAQTAIPEGTVIGDGKLKINLARIDT 176

Query: 172 RLIHGQVATRWTKETNVSRIIVVSDEVAADTVRKTLLTQVAPPGVTAHVVDVAKMIRVYN 231
           RL+HGQVAT WT ++   RIIV SD V+ D++RK L+ Q AP  V A+VV + K+I    
Sbjct: 177 RLLHGQVATAWTPDSKADRIIVASDSVSQDSLRKELIKQAAPGNVKANVVPIDKLIAAAK 236

Query: 232 NPKYAGERVMLLFTNPTDVERLVEGGVKITSVNVGGMAFRQGKTQVNNAVSVDEKDIEAF 291
           +P++ G   ++LF  P D  R +EGGV I ++NVG MA   GKT VNN +S+D+ D+  F
Sbjct: 237 DPRFGGTHALILFETPQDALRAIEGGVPIKTLNVGSMAHSTGKTMVNNVLSMDKDDVATF 296

Query: 292 KKLNARGIELEVRKVSTDPKLKMMDLISK 320
           +KL   G+  +VRKV  D K  + DLI+K
Sbjct: 297 EKLRDLGVTFDVRKVPNDSKKDLFDLINK 325


Lambda     K      H
   0.316    0.133    0.375 

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: 231
Number of extensions: 9
Number of successful extensions: 3
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: 323
Length of database: 329
Length adjustment: 28
Effective length of query: 295
Effective length of database: 301
Effective search space:    88795
Effective search space used:    88795
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