GapMind for catabolism of small carbon sources

 

Alignments for a candidate for alr in Klebsiella michiganensis M5al

Align lysine racemase (EC 5.1.1.5) (characterized)
to candidate BWI76_RS17730 BWI76_RS17730 alanine racemase

Query= BRENDA::Q04HB7
         (371 letters)



>FitnessBrowser__Koxy:BWI76_RS17730
          Length = 356

 Score =  127 bits (320), Expect = 4e-34
 Identities = 114/372 (30%), Positives = 177/372 (47%), Gaps = 26/372 (6%)

Query: 7   RSTRIEFSKSSLAYNVQYTKQVSGAKTLWLAVKSNAYGHGLLQVSKIARECGVDGLAVSV 66
           R  +     S+L  N Q  ++ + A  LW  VK+NAYGHGL +V         DG A+  
Sbjct: 3   RPVKASIDMSALRQNQQIVRRAAPASRLWAVVKANAYGHGLARVWNALS--AADGFAMLN 60

Query: 67  LDEGIAIRQAGIDDFILIL-GPIDVKYAPIASKYHFLTTVSSLDWLKSADKILGKEKLSV 125
           L+E I +R+ G    IL+L G        +  KY   T+V S   +K+  +      L +
Sbjct: 61  LEEAILLRELGWKGPILMLEGFFHADELALFDKYRLTTSVHSNWQIKALQQAKLHAPLDI 120

Query: 126 NLAVDTGMNRIGVRSKKDLKDEIEFLQEHSDH-FSYDGIFTHFASSDNPDDHYFQRQKNR 184
            + V++GMNR+G    +     I + Q  S H  S   + +HFA ++NPD         R
Sbjct: 121 YVKVNSGMNRLGFMPDRL---HIVWQQLRSLHNVSEMTLMSHFAEAENPDG--IVEPMRR 175

Query: 185 WYELIDGLIMPRYVHVMNSGAAMYHSKELPGCNSIARVGTVVYGVEPSEGVLGPIDK--L 242
             +  +GL  PR   + NS A ++H +      +  R G V+YG  PS G+   +    L
Sbjct: 176 IEQAAEGLDCPR--SLANSAATLWHPESH---FNWVRPGIVLYGASPS-GLWQDVANTGL 229

Query: 243 KPVFELKSALTFVKKIPAGEGISYGSKFVTSRDTWIGTLPIGYGDGW--LAEYQDFQLLI 300
           KPV  L S +  V+ + AGE + YG+ + T+ +  IG +  GY DG+  LA      +L+
Sbjct: 230 KPVMTLSSEIIAVQNLKAGEAVGYGATWRTAEERRIGIVACGYADGYPRLAP-SGTPVLV 288

Query: 301 DGQKCRQVGQIAMDQMMVALP--HEYPIGTEVTLIGKSGKYENTLYDLHKHSGVPPWKIT 358
           DG +   VG+I+MD + V L    +  IG  V L GK  K +    D+    G   +++ 
Sbjct: 289 DGVRTATVGRISMDMLAVDLTPCPQAGIGAPVELWGKEIKID----DVASACGTVGYELM 344

Query: 359 VAFSDRLKRMVV 370
            A + R+  + V
Sbjct: 345 CALAPRVPVVTV 356


Lambda     K      H
   0.319    0.137    0.410 

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: 328
Number of extensions: 21
Number of successful extensions: 6
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: 371
Length of database: 356
Length adjustment: 29
Effective length of query: 342
Effective length of database: 327
Effective search space:   111834
Effective search space used:   111834
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: 49 (23.5 bits)

This GapMind analysis is from Sep 17 2021. The underlying query database was built on Sep 17 2021.

Links

Downloads

Related tools

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