GapMind for catabolism of small carbon sources

 

Alignments for a candidate for natD in Thiothrix lacustris DSM 21227

Align NatD, component of The neutral amino acid permease, N-1 (transports pro, phe, leu, gly, ala, ser, gln and his, but gln and his are not transported via NatB) (characterized)
to candidate WP_028487960.1 Q394_RS0102915 branched-chain amino acid ABC transporter permease

Query= TCDB::Q8YXD0
         (288 letters)



>NCBI__GCF_000621325.1:WP_028487960.1
          Length = 310

 Score =  150 bits (379), Expect = 3e-41
 Identities = 104/305 (34%), Positives = 165/305 (54%), Gaps = 26/305 (8%)

Query: 1   MDIQTIQLIVNGIAVGSIIALAAVGLTLTYGILRLSNFAHGDFLTLGAYLTFFV--NTFG 58
           MDI   QL VNG+ +GS+ AL A+G TL YGIL L NFAHG+   +G+ +   V    FG
Sbjct: 1   MDIFAQQL-VNGLVLGSVYALVALGYTLVYGILELINFAHGETTMMGSMIALAVIGALFG 59

Query: 59  V-----NIWLSMIVAVVGTVGVMLLSEKLLWSRMRSIR-ANSTTLIIISIGLALFLRNGI 112
           V      I + +   +V     MLL   +     R +R A     +I +IG+++ L+N  
Sbjct: 60  VAPDLPGILIVLAGLLVAIPACMLLGYSIERVAYRPLRHAPRLAPLITAIGMSIVLQNVA 119

Query: 113 ILIWGGRNQNYNLPITP--ALDIFGVKVPQNQLLVLALAVLSIGALHYLLQNTKIGKAMR 170
           +LIWG +   +   + P    D+FG  +   Q+ +L L V  +  L  L+  T++G+AMR
Sbjct: 120 MLIWGKQYIAFPTTLLPQGRHDVFGASITDVQIAILVLTVTIMAGLVTLVNRTRLGRAMR 179

Query: 171 AVADDLDLAKVSGIDVEQVIFWTWLIAGTVTSLGGSM----YGLITAVRPNMGWFLILPL 226
           A A    +A++ G++V +VI  T++I   + ++ G M    YG        MG+ L L  
Sbjct: 180 ATAQAPAVAQLMGVNVNRVISATFVIGAALAAIAGVMVSANYG---QAHYYMGFLLGLKA 236

Query: 227 FASVILGGIGNPYGAIAAAFIIGIVQ--------EVSTPFLGSQYKQGVALLIMILVLLI 278
           F++ +LGGIGN  GA+    ++G+++        +++  FLGS Y+   A L++ILVL +
Sbjct: 237 FSAAVLGGIGNLAGAMLGGLLLGVIEALGAGYIGDLTGGFLGSNYQDIFAFLVLILVLTL 296

Query: 279 RPKGL 283
           +P GL
Sbjct: 297 KPSGL 301


Lambda     K      H
   0.328    0.144    0.426 

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: 259
Number of extensions: 19
Number of successful extensions: 5
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: 288
Length of database: 310
Length adjustment: 27
Effective length of query: 261
Effective length of database: 283
Effective search space:    73863
Effective search space used:    73863
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 15 ( 7.1 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 40 (21.7 bits)
S2: 48 (23.1 bits)

This GapMind analysis is from Apr 09 2024. 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