GapMind for catabolism of small carbon sources

 

Alignments for a candidate for Psest_0085 in Thermodesulforhabdus norvegica DSM 9990

Align alpha-ketoglutarate TRAP transporter, solute receptor component (characterized)
to candidate WP_093392797.1 BM091_RS01090 TRAP transporter substrate-binding protein

Query= reanno::psRCH2:GFF85
         (317 letters)



>NCBI__GCF_900114975.1:WP_093392797.1
          Length = 336

 Score =  163 bits (412), Expect = 6e-45
 Identities = 116/332 (34%), Positives = 173/332 (52%), Gaps = 20/332 (6%)

Query: 5   KRLGLLAAAAAFTAS-TAAVAAPTFINILTGGTSGVYYPIGVALSQQYNKIDGAKTSVQA 63
           ++L +L  A    A  + A A+   + I TGG  GVYY  G  +++  +K    + +   
Sbjct: 6   RKLTILIFALTLVAGFSQAEASKVRLVIGTGGLGGVYYYYGTTVAEIISKAGEFEATAMQ 65

Query: 64  TKASVENLNLLQAGRGE------LAFSLGDSVEDAWNGVEDAGFKAPLKRLRAIAGTYNN 117
           T ASV+NL L+Q           LA  L DS   A+ G  +     P K +R +   Y N
Sbjct: 66  TAASVDNLQLIQKRTDPEGNVYYLACVLPDSAYLAYTGQHEKFKDQPAKDVRILWTMYPN 125

Query: 118 YIQIVASAESGIKTLDDLKGKRISVGAPKSGTELNARAIFKAAGLDYKDMGRVEFLPYAE 177
           Y+ IV    SGI+T+ DLKGKR+S GAP SGTE+ A  + +AAG+   D  + E L  +E
Sbjct: 126 YLHIVTKEGSGIETVADLKGKRVSTGAPGSGTEVEAFMVLEAAGISTSDFAKHERLGASE 185

Query: 178 SVELIKNRQLDATLQSSGLGMAAIRDLASTM-----PVTFVEIPA--EVVEKIES---DA 227
           S E +    +DA   S GL  ++I +LA+T+      +  + +PA  ++V+ I S     
Sbjct: 186 SAEALSAGTIDAYFWSGGLPTSSITELATTLKRKGSKIKLIGLPADGDIVKNIASKFPGV 245

Query: 228 YLAGVIPAGTYDGQDADVPTVAITNILVTHEKVSDEVAYQMTKLMFDNLAALGNAHSAAK 287
                I A  Y G   D PT+A  N+ +    + +EVAY++TK +F+ L  L +A   +K
Sbjct: 246 CEPATIAASVY-GTSEDTPTLAFWNLFMGPASLPEEVAYKITKTVFEKLEELHSAVKPSK 304

Query: 288 DIKLENATKNL--PIPLHPGAERFYKEAGVLK 317
               ENA K +   IP HPG+ +++KE GVLK
Sbjct: 305 ATTPENAVKFVGGTIPYHPGSLKYFKEIGVLK 336


Lambda     K      H
   0.314    0.131    0.359 

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: 227
Number of extensions: 9
Number of successful extensions: 4
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: 317
Length of database: 336
Length adjustment: 28
Effective length of query: 289
Effective length of database: 308
Effective search space:    89012
Effective search space used:    89012
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: 42 (22.0 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