GapMind for catabolism of small carbon sources

 

Alignments for a candidate for ilvE in Halomonas desiderata SP1

Align L-leucine transaminase; L-isoleucine transaminase (EC 2.6.1.42) (characterized)
to candidate WP_086511056.1 BZY95_RS16860 PLP-dependent aminotransferase family protein

Query= reanno::acidovorax_3H11:Ac3H11_1358
         (401 letters)



>NCBI__GCF_002151265.1:WP_086511056.1
          Length = 455

 Score =  132 bits (333), Expect = 2e-35
 Identities = 92/311 (29%), Positives = 154/311 (49%), Gaps = 15/311 (4%)

Query: 73  QYAASEGYAPLRQAIADFLPW---DVDADQILITTGSQQALDLIAKVLIDENSRVLVETP 129
           +Y   +G+ PLR AIA  L         +Q+L+T G+  A DLI +  +D    VLVETP
Sbjct: 135 EYGMPQGFEPLRDAIARVLAGRSIHAAPEQVLLTFGANHAFDLIIRHFVDAGDSVLVETP 194

Query: 130 TYLGALQAFTPMEPSVVAVASDDEGVLIDDLKAKVGTGADKARFLYVLPNFQNPTGRTMT 189
            Y             +V V+   +G  +++ + KV     + R  ++ PN  NPTG +M+
Sbjct: 195 GYYPLFGKLRLARAKLVGVSRTAKGPDLEEFERKVRQY--RPRLFFLQPNAHNPTGTSMS 252

Query: 190 EARRAALVKAAAELNLPLVEDNPYGDLWFDNPPPAPLTARNP-EGCIYMGSFSKVLAPGL 248
            +    L+K A +  + LVED+ + DL       A L A +  E  IY+G+FSK L+ GL
Sbjct: 253 LSNMHQLLKIAEQYGVVLVEDDVFADLLPQGS--AHLAALDGLENVIYVGTFSKTLSTGL 310

Query: 249 RLGFVVAPKAVYPKLLQAKQAADLHTPGYNQRLVAEVMKGNFLDRHVPTIRALYKQQCEA 308
           R G++   +A+   L   K    +++  + + ++ E++      RH+  +R    +   +
Sbjct: 311 RSGYIAGSRALIRSLTDIKMLTVVNSSTFIESVIHELIVKGRYRRHLVQLRERVAKASAS 370

Query: 309 MLAALTQEMAGLGVE-WNRPDGGMFLWVRLPEGMSAIELLPQAVERNVAFVPGAAF--YA 365
              AL +    +G++  + P GG +LW RLP G++ +EL  +A E  +   PGA F    
Sbjct: 371 AQRALRE----VGIDDVSGPGGGYYLWARLPAGLNTLELAKRATEEGIFIAPGAIFSLRP 426

Query: 366 DNADPRTLRLS 376
           D  D   +R++
Sbjct: 427 DGIDGTAMRIN 437


Lambda     K      H
   0.318    0.134    0.392 

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: 382
Number of extensions: 24
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: 401
Length of database: 455
Length adjustment: 32
Effective length of query: 369
Effective length of database: 423
Effective search space:   156087
Effective search space used:   156087
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 (21.7 bits)
S2: 51 (24.3 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