GapMind for catabolism of small carbon sources

 

Alignments for a candidate for aapJ in Desulfacinum infernum DSM 9756

Align ABC transporter for L-Glutamine, L-Histidine, and other L-amino acids, periplasmic substrate-binding component (characterized)
to candidate WP_073037857.1 BUB04_RS05915 amino acid ABC transporter substrate-binding protein

Query= reanno::Smeli:SMc02118
         (341 letters)



>NCBI__GCF_900129305.1:WP_073037857.1
          Length = 337

 Score =  395 bits (1015), Expect = e-115
 Identities = 193/339 (56%), Positives = 249/339 (73%), Gaps = 3/339 (0%)

Query: 3   RRILTALVGAAVVGIGTHAASAATLDDVKAKGFVQCGVNTGLAGFAAPDASGNWSGFDVD 62
           +RI   +V  AV+ +    A+A TLD+VKA+G++  GVN  + GF+ PD  G W G DVD
Sbjct: 2   KRIRIFVVLLAVLALAL-PANAGTLDEVKARGYLIAGVNGSVFGFSMPDEKGVWKGLDVD 60

Query: 63  YCKAIAAAIFGDGSKVKYTPLSAKERFPALQSGEVDVLARNTTWSINRDTALGFNFRPVN 122
             +AIAAA+FGD +K+K+ PL+A +R PALQS E+DVL RNTT ++ R+T  G NF  VN
Sbjct: 61  TARAIAAAVFGDANKIKFVPLTAVQRLPALQSKEIDVLCRNTTQTLTRETTNGLNFVHVN 120

Query: 123 YYDGQGFMVRKELDVKSALELSGAAVCVQTGTTTELNLADYFKANNLQYNPVVFEKLEEV 182
           +YDGQGFMV K+L VKSA EL GA VCV  GTTTELN AD+F+ NN+Q+ PVV E+  E+
Sbjct: 121 FYDGQGFMVPKKLGVKSAKELDGATVCVLPGTTTELNAADFFRKNNMQWKPVVIEQAAEL 180

Query: 183 NAAYDAGRCDVYTTDQSGLYSLRLTLSKPDDHIVLPEIISKEPLAPAVRQGDDQWFDIVS 242
           N A+ AGRCDV T+D S L   R     P+++++LPE+ISKEPLAP VR GDDQW+DIV+
Sbjct: 181 NKAFFAGRCDVLTSDVSQLAGHRAVAPDPNEYVILPEVISKEPLAPVVRHGDDQWYDIVN 240

Query: 243 WVHYALVQAEEFGVTQANLEEMKKSTNPDVQRFLGVEADSKIGTDLGLTNEWAVNIVKAV 302
           W   AL+QAEEFG+T  N++EM KS +P++QRFLGV     +G  LGL  +WA NI+K V
Sbjct: 241 WTVMALIQAEEFGITSQNVDEMLKSNDPEIQRFLGVTPG--MGAALGLDEKWAYNIIKQV 298

Query: 303 GNYGEVFDRNIGAGSPLKIERGLNALWNKGGLQYAPPVR 341
           GNYGE+F+RN+G  +PL +ERGLNALW +GGL YA P R
Sbjct: 299 GNYGEIFERNVGPNTPLAMERGLNALWTQGGLMYAAPFR 337


Lambda     K      H
   0.317    0.134    0.399 

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: 373
Number of extensions: 14
Number of successful extensions: 2
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: 341
Length of database: 337
Length adjustment: 28
Effective length of query: 313
Effective length of database: 309
Effective search space:    96717
Effective search space used:    96717
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.

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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