GapMind for catabolism of small carbon sources

 

Alignments for a candidate for Dshi_1195 in Marivita geojedonensis DPG-138

Align TRAP transporter solute receptor (characterized, see rationale)
to candidate WP_085636379.1 MGEO_RS08945 TAXI family TRAP transporter solute-binding subunit

Query= uniprot:A8LI83
         (330 letters)



>NCBI__GCF_002115805.1:WP_085636379.1
          Length = 329

 Score =  569 bits (1467), Expect = e-167
 Identities = 279/326 (85%), Positives = 297/326 (91%), Gaps = 1/326 (0%)

Query: 6   MTGTAMAVALSATVVTTATAQ-DRDGWPDSFTVGTASQGGTYFAYGSGWANLVAEELGLS 64
           +T    AVA++ T    A +  DR+GWP+SFTVGTASQGGTYFAYGSGWANLVAEELG+S
Sbjct: 4   ITAITFAVAVAVTGQANAGSHVDREGWPESFTVGTASQGGTYFAYGSGWANLVAEELGVS 63

Query: 65  GGGEVTGGPMQNMALVHTGDAQFGMTTMGPAAESLAGTNPIAPGLQMDNACAMFPMYQTP 124
           GGGEVTGGPMQNMALVHTGDAQFGMTTMGPAAESL GTNPIAPGLQM NACAMFPMYQTP
Sbjct: 64  GGGEVTGGPMQNMALVHTGDAQFGMTTMGPAAESLGGTNPIAPGLQMTNACAMFPMYQTP 123

Query: 125 FSVTALSSSGIASIADIPDGAKIGFGPAGSTSDTYFPRMMEALGVNFERRNGGWSDLGGQ 184
           FSVTALSSSGI+SI+DIP+GA+IGFGPAGSTSDTYFPRMME LGVNFERRNGGWSDLGGQ
Sbjct: 124 FSVTALSSSGISSISDIPEGARIGFGPAGSTSDTYFPRMMEELGVNFERRNGGWSDLGGQ 183

Query: 185 LQDGLLDVIAFAAGVPVPAVSQLEVQTDINIIEFTEEEQAKIMADFPVSEFSIGAGTYST 244
           LQDGLLDVIAFAAGVPVPAVSQLEVQTD+NIIEFTEEEQA+IM  FPVS F I A TY+T
Sbjct: 184 LQDGLLDVIAFAAGVPVPAVSQLEVQTDVNIIEFTEEEQAQIMEAFPVSAFEIAADTYTT 243

Query: 245 LEADARSVSMWNFAIANCDLPASFVKAATDVVMSDNARMVGIHKAARSTLPENWDKNKVL 304
           LEA ARSVSMWNFAIANC+LPASFV A  DVVMSDN RMV IH+AARSTLPENWDKN VL
Sbjct: 244 LEAPARSVSMWNFAIANCELPASFVNAVVDVVMSDNERMVNIHRAARSTLPENWDKNGVL 303

Query: 305 KWHPGAAEWFKENAGADIPDDMIHGM 330
           KWHPGAA+WFK+NAGADIPD MIHGM
Sbjct: 304 KWHPGAAQWFKDNAGADIPDSMIHGM 329


Lambda     K      H
   0.316    0.131    0.393 

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: 441
Number of extensions: 13
Number of successful extensions: 1
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: 330
Length of database: 329
Length adjustment: 28
Effective length of query: 302
Effective length of database: 301
Effective search space:    90902
Effective search space used:    90902
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: 49 (23.5 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