GapMind for catabolism of small carbon sources

 

Alignments for a candidate for L-LDH in Burkholderia phytofirmans PsJN

Align L-lactate dehydrogenase (cytochrome) (EC 1.1.2.3) (characterized)
to candidate BPHYT_RS31690 BPHYT_RS31690 hypothetical protein

Query= reanno::Smeli:SM_b20850
         (378 letters)



>FitnessBrowser__BFirm:BPHYT_RS31690
          Length = 383

 Score =  216 bits (549), Expect = 1e-60
 Identities = 125/372 (33%), Positives = 198/372 (53%), Gaps = 4/372 (1%)

Query: 7   IRDLKALARRRVPKLFFDYADSGAWTEGTYRANEEDFAG-IKLRQRVLVDMSDRSLETTM 65
           +RD    AR+ +P   F+    GA  +     NE  F     + +R     +D++   T+
Sbjct: 1   MRDFVEPARKHLPAFAFNTLAGGAGNDAGVAENEAAFGRRFFVSRRFAPASTDQT--ATV 58

Query: 66  IGQKVSMPVALAPTGLTGMQHADGEMLAAQAAEAFGVPFTLSTMSICSIEDVASVTTKPF 125
            G   + P  +AP GL  + +   ++L AQAA+A   PF LST +  SIE +  V     
Sbjct: 59  FGHSYASPFGVAPMGLANLFYPGADLLLAQAAQAGNFPFVLSTAASTSIERITKVAPDVS 118

Query: 126 WFQLYVMREREFVLDLIDRAKAAKCSALVMTLDLQILGQRHKDLRNGLSAPPRLTPKHLW 185
           W+QLY++ +     +L+ R      + LV+T+D+ + G+R+  +R+G++ P R T   L 
Sbjct: 119 WYQLYLLSDDRLNAELLSRVAGCGVAVLVLTVDVPVAGRRNSAIRDGVTLPLRWTSALLA 178

Query: 186 MMATRPGWCMKMLGTNRRTFRNIVGHAKSVADLSSLQAWTNEQFDPQLSWKDVEWIKERW 245
            +  RP W + ML        N   HA   AD+ +            L W D++ ++  W
Sbjct: 179 DVMRRPQWALGMLRHGAPKLENYAPHA-GTADVGAASRHIASVMKMGLEWDDLKKVRAMW 237

Query: 246 GGPLILKGILDPEDAKMAAKTGADAIIVSNHGGRQLDGAHSSISMLPRIVEAVGDQIEVH 305
            G L++KGIL P+DA  +   GAD I VSNHGGRQL+GA +S+  L  I  AVG    V 
Sbjct: 238 PGKLVIKGILHPDDAARSVALGADGIWVSNHGGRQLEGAIASLDALSEIRRAVGRDTAVF 297

Query: 306 LDGGIRSGQDVLKAIALGAKGTYIGRPFLYGLGALGKEGVTLALDIIRKEMDTTMALCGK 365
           LDGG+R+G+D+LKA ALGA   + GR F + + A G+ GV  A++I+++E+   +A  G 
Sbjct: 298 LDGGVRTGEDILKACALGAGLCFSGRSFAFPVAAYGERGVRAAVEILKEEIRVGLAQLGV 357

Query: 366 RRITEVGRDIIA 377
           + ++ +  D ++
Sbjct: 358 QSLSALTSDSLS 369


Lambda     K      H
   0.321    0.136    0.406 

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: 334
Number of extensions: 17
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: 378
Length of database: 383
Length adjustment: 30
Effective length of query: 348
Effective length of database: 353
Effective search space:   122844
Effective search space used:   122844
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 (21.9 bits)
S2: 50 (23.9 bits)

This GapMind analysis is from Sep 17 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