GapMind for catabolism of small carbon sources

 

Alignments for a candidate for pta in Oleispira antarctica

Align ethanolamine utilization protein eutD (characterized)
to candidate WP_046008430.1 OLEAN_RS05710 phosphate acetyltransferase

Query= CharProtDB::CH_024378
         (338 letters)



>NCBI__GCF_000967895.1:WP_046008430.1
          Length = 326

 Score =  322 bits (824), Expect = 1e-92
 Identities = 163/320 (50%), Positives = 224/320 (70%), Gaps = 2/320 (0%)

Query: 2   IIERCRELALRAPARVVFPDALDQRVLKAAQYLHQQGLATPILVANPFELRQFALSHGVA 61
           ++++CR    ++P R+VF D+LD RVL+AA  L +QGLA PIL+ NPFE+R +A  +G+A
Sbjct: 3   VVQQCRTECKQSPQRIVFADSLDVRVLQAANELQKQGLAEPILIGNPFEIRDYAYRNGIA 62

Query: 62  MDGLQVIDPHGNLAMREEFAHRWLARAGEKTPPDALEKLT-DPLMFAAAMVSAGKADVCI 120
           M    V+DP  +    E F + +L  +   T  D+ E L   PL +AA MV   +ADVCI
Sbjct: 63  MPCFAVVDPERS-GYLEPFVNAYLENSDANTERDSAEALLRKPLFYAAMMVKQNQADVCI 121

Query: 121 AGNLSSTANVLRAGLRIIGLQPGCKTLSSIFLMLPQYSGPALGFADCSVVPQPTAAQLAD 180
           AGNLS++ +VLRA L++IG+    +T+SS F+M          FAD +VVP+PT  QLAD
Sbjct: 122 AGNLSTSGDVLRAALKVIGIAEQHRTVSSFFVMTSPDGSDVRLFADAAVVPEPTVEQLAD 181

Query: 181 IALASAETWRAITGEEPRVAMLSFSSNGSARHPCVANVQQATEIVRERAPKLVVDGELQF 240
           I + +A  +  +TGE+ RVAMLSFSS GS+ HP   +V++A ++VR ++P L+VDGELQF
Sbjct: 182 ITIDTARNFEKLTGEKARVAMLSFSSKGSSNHPAAVHVREAFDLVRRKSPDLIVDGELQF 241

Query: 241 DAAFVPEVAAQKAPASPLQGKANVMVFPSLEAGNIGYKIAQRLGGYRAVGPLIQGLAAPM 300
           DAA  P VA  KAP SPL G +NVM+FPSL AGNI YK+AQRL  Y+A+GPL+QGL  PM
Sbjct: 242 DAAVDPIVADHKAPDSPLHGSSNVMIFPSLNAGNIAYKVAQRLAHYQALGPLLQGLRKPM 301

Query: 301 HDLSRGCSVQEIIELALVAA 320
           HDLSRGCS  +I+++A++A+
Sbjct: 302 HDLSRGCSADDIVDIAILAS 321


Lambda     K      H
   0.320    0.134    0.387 

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: 308
Number of extensions: 10
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: 338
Length of database: 326
Length adjustment: 28
Effective length of query: 310
Effective length of database: 298
Effective search space:    92380
Effective search space used:    92380
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.4 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 41 (21.8 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