GapMind for catabolism of small carbon sources

 

Alignments for a candidate for gcdG in Sphingomonas histidinilytica UM2

Align succinyl-CoA-glutarate CoA-transferase (EC 2.8.3.13) (characterized)
to candidate WP_079647927.1 B5X82_RS09500 CoA transferase

Query= reanno::pseudo5_N2C3_1:AO356_10845
         (406 letters)



>NCBI__GCF_900167915.1:WP_079647927.1
          Length = 372

 Score =  411 bits (1057), Expect = e-119
 Identities = 213/366 (58%), Positives = 262/366 (71%), Gaps = 10/366 (2%)

Query: 4   LSHLRVLDLSRVLAGPWAGQILADLGADVIKVERPGNGDDTRAWGPPFLKDARGENTTEA 63
           L+ L+V++L+R+LAGPWAGQ+LADLGA+VIKVE P  GDDTR WGPPF+   R + + +A
Sbjct: 6   LAGLKVVELARILAGPWAGQVLADLGAEVIKVESPA-GDDTRGWGPPFID--RADGSRDA 62

Query: 64  AYYLSANRNKQSVTIDFTRPEGQRLVRELAAKSDILIENFKVGGLAAYGLDYDSLKAINP 123
           AY+ +ANR K+S  +DF   +GQR VREL A +D++IENFKVGGLA YGLD+ SL AINP
Sbjct: 63  AYFHAANRGKRSEAVDFATEQGQRRVRELVADADVVIENFKVGGLAKYGLDHASLAAINP 122

Query: 124 QLIYCSITGFGQTGPYAKRAGYDFMIQGLGGLMSLTGRPEGDEGAGPVKVGVALTDILTG 183
           +L+YCSITGFGQ GPYA RAGYDF+IQG+GG+M LTG P+G     P K+GVA  DILTG
Sbjct: 123 RLVYCSITGFGQDGPYAARAGYDFIIQGMGGIMDLTGEPDG----APQKIGVAYADILTG 178

Query: 184 LYSTAAILAALAHRDHVGGGQHIDMALLDVQVACLANQAMNYLTTGNAPKRLGNAHPNIV 243
           LY+   I AALA R+  G GQH+DMALLDV V  LANQAMNYL +G AP RLGNAHPNIV
Sbjct: 179 LYAVIGIQAALAERERSGLGQHVDMALLDVMVGTLANQAMNYLASGVAPTRLGNAHPNIV 238

Query: 244 PYQDFPTADGDFILTVGNDGQFRKFAEVAGQPQWADDPRFATNKVRVANRAVLIPLIRQA 303
           PYQ +PT D  FIL  GND Q+ +F +V G     D   F TN  R+A R  L  +I  A
Sbjct: 239 PYQAYPTQDDWFILATGNDRQYERFCDVVGIAPGDD---FKTNPQRLARRDALSAIIADA 295

Query: 304 TVFKTTAEWVTQLEQAGVPCGPINDLAQVFADPQVQARGLAMELPHLLAGKVPQVASPIR 363
           T     A+ +  LE+ GVP GPIND+AQ  ADPQV  RG+ +++     G VP +  PIR
Sbjct: 296 TRRWPRADLLAALERVGVPAGPINDVAQALADPQVVHRGMVVDMVDEDGGHVPGMRLPIR 355

Query: 364 LSETPV 369
            S +P+
Sbjct: 356 FSRSPL 361


Lambda     K      H
   0.319    0.137    0.408 

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: 531
Number of extensions: 23
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: 406
Length of database: 372
Length adjustment: 30
Effective length of query: 376
Effective length of database: 342
Effective search space:   128592
Effective search space used:   128592
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 (21.7 bits)
S2: 50 (23.9 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