GapMind for catabolism of small carbon sources

 

Alignments for a candidate for odc in Sulfurivirga caldicuralii DSM 17737

Align Lysine/ornithine decarboxylase; LDC; EC 4.1.1.17; EC 4.1.1.18 (uncharacterized)
to candidate WP_084188303.1 BUQ81_RS07475 type III PLP-dependent enzyme

Query= curated2:O50657
         (393 letters)



>NCBI__GCF_900141795.1:WP_084188303.1
          Length = 394

 Score =  248 bits (634), Expect = 2e-70
 Identities = 142/371 (38%), Positives = 216/371 (58%), Gaps = 14/371 (3%)

Query: 6   LSEKEVKTLAKRIPTPFLVASLDKVEENYQFMRRHLPRAGVFYAMKANPTPEILSLLAGL 65
           L  + ++ LA+   TP LV +L +V+E YQ ++  LP   +FYA+KA   P +L  L  L
Sbjct: 22  LDRQTLRQLAQIHGTPLLVLNLKRVDEQYQRLQAALPGVKLFYAVKALAHPALLMRLNQL 81

Query: 66  GSHFDVASAGEMEILHELGVDGSQMIYANPVKDARGLKAAADYNVRRFTFDDPSEIDKMA 125
           G HFD+A+AGE+ ++ +LG+   + I+ +P+K    ++ A D+   RF  D+ +E+DK  
Sbjct: 82  GGHFDLATAGEVNMVRDLGIVAERCIHTHPIKKDSEIREALDFGCTRFVVDNLAEVDKFV 141

Query: 126 KAVPGADVLVRIAVRNNKALVDLNTKFGAPVEEALDLLKAAQDAGLHAMGICFHVGSQSL 185
                  ++VR++ R+  A+VDL+ KFG  +EE   LL+ AQ  GL   G+ FHVGSQS 
Sbjct: 142 PYKDRVQLIVRVSYRSQDAVVDLSRKFGCALEELHTLLEHAQTQGLTIHGLSFHVGSQSG 201

Query: 186 STAAYE---EALLVARRLFDEAEEMGMHLTDLDIGGGFPVPDAKGLNVDLAAMMEAINKQ 242
           S AA+    EA + A R FD+ +        LDIGGGFPV     + +++      I + 
Sbjct: 202 SPAAHVKAIEASIEAMRTFDQIDWKW-----LDIGGGFPVSYQTPV-MEIEDFCAPIREA 255

Query: 243 IDRLFPDTAVWTEPGRYMCGTAVNLVTSVIGTKTRGEQPWYILDEGIYGCFSGIMYDHWT 302
           + ++  +  +W EPGRY+   ++  +  V+G   RG + WY LD+G+YG  SG +YDH  
Sbjct: 256 LAQVPENIEIWAEPGRYIAAPSMVELLCVMGRARRGTRMWYYLDDGVYGALSGQIYDHAL 315

Query: 303 YPLHCF---GKGNKKPSTFGGPSCDGIDVLYRDFMAPELKIGDKVLVTEMGSYTSVSATR 359
           YP+ C     + + +PS   GP+CD IDV+  D   PEL+IGD ++   MG+YT  SAT 
Sbjct: 316 YPI-CLLEPREDDLQPSVLAGPTCDSIDVIDEDIDLPELQIGDLLVARMMGAYTLASATE 374

Query: 360 FNGFYLAPTII 370
           FN FY  P ++
Sbjct: 375 FN-FYPKPQVV 384


Lambda     K      H
   0.320    0.137    0.407 

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: 369
Number of extensions: 12
Number of successful extensions: 4
Number of sequences better than 1.0e-02: 1
Number of HSP's gapped: 2
Number of HSP's successfully gapped: 1
Length of query: 393
Length of database: 394
Length adjustment: 31
Effective length of query: 362
Effective length of database: 363
Effective search space:   131406
Effective search space used:   131406
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: 50 (23.9 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