GapMind for catabolism of small carbon sources

 

Alignments for a candidate for Psest_0085 in Calditerrivibrio nitroreducens DSM 19672

Align alpha-ketoglutarate TRAP transporter, solute receptor component (characterized)
to candidate WP_013450664.1 CALNI_RS02695 C4-dicarboxylate ABC transporter substrate-binding protein

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



>NCBI__GCF_000183405.1:WP_013450664.1
          Length = 324

 Score =  163 bits (413), Expect = 5e-45
 Identities = 109/329 (33%), Positives = 171/329 (51%), Gaps = 19/329 (5%)

Query: 3   LTKRLGLLAAAAAFTASTAAVAAPTFINILTGGTSGVYYPIGVALSQ-------QYNKID 55
           + K L +L A +   + +   A  TF+ I TGG +GVYYP+G A+++       QYN   
Sbjct: 1   MKKILVMLMAFSVIFSGSIFAAKQTFVTIGTGGVTGVYYPVGGAIARLVNAKKAQYN--- 57

Query: 56  GAKTSVQATKASVENLNLLQAGRGELAFSLGDSVEDAWNGVEDAGFKAPLKRLRAIAGTY 115
             K +V++T  SV N+N + +G  E   +  D    A++G      K   K+L  + G +
Sbjct: 58  -IKATVESTGGSVYNINSVLSGDLEFGIAQADLTYQAYHGQGAWKDKGAQKKLAVVFGLH 116

Query: 116 NNYIQIVASAESGIKTLDDLKGKRISVGAPKSGTELNARAIFKAAGLDYKDMGRVEFLPY 175
           N ++ +VASA SGI  + DLKGKR+++G   SG   N+R + KA GL   D+ + E++  
Sbjct: 117 NEFVTLVASANSGINGIPDLKGKRVNLGGVGSGQLENSRDLLKAFGLKESDL-KAEYIKP 175

Query: 176 AESVELIKNRQLDATLQSSGLGMAAIRDLAS-TMPVTFVEIPAEVVEKI--ESDAYLAGV 232
            ES  LI++ +LDA   + G    ++ +  S  + V  V I    VEK+  E   Y  G 
Sbjct: 176 VESAGLIQDERLDAFFYTVGHPNGSVSEATSGRIKVKIVPITGTPVEKLIKELPYYSKGY 235

Query: 233 IPAGTY----DGQDADVPTVAITNILVTHEKVSDEVAYQMTKLMFDNLAALGNAHSAAKD 288
           IP   Y    + +D  VP++ I  +LVT   V  +V Y +TK + +N+      H A   
Sbjct: 236 IPVSLYPNAANAKDGKVPSIGIQALLVTSTDVPADVVYAITKEVVENIQEFKKLHPALGG 295

Query: 289 IKLENATKNLPIPLHPGAERFYKEAGVLK 317
           + +E+       PLHPGA +++KE G+ K
Sbjct: 296 LDIEDMVNVNVAPLHPGALKYFKEKGLKK 324


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: 246
Number of extensions: 13
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: 317
Length of database: 324
Length adjustment: 28
Effective length of query: 289
Effective length of database: 296
Effective search space:    85544
Effective search space used:    85544
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.

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