GapMind for catabolism of small carbon sources

 

Alignments for a candidate for atoB in Sulfuritalea hydrogenivorans DSM 22779

Align Acetyl-CoA acetyltransferase; Acetoacetyl-CoA thiolase; EC 2.3.1.9 (characterized)
to candidate WP_041100093.1 SUTH_RS13985 3-oxoadipyl-CoA thiolase

Query= SwissProt::Q0AVM3
         (396 letters)



>NCBI__GCF_000828635.1:WP_041100093.1
          Length = 402

 Score =  321 bits (822), Expect = 3e-92
 Identities = 181/402 (45%), Positives = 250/402 (62%), Gaps = 10/402 (2%)

Query: 1   MTREVVLVGACRTPVGTFGGTLKDVGSAQLGAIVMGEAIKRAG-IKAEQIDEVIFGCVLQ 59
           MT +  +  A RTP+G +GGTL  + +  LGA+ +   + R G +  E++DEVI+GC  Q
Sbjct: 1   MTEQAFICDAVRTPIGRYGGTLSGIRTDDLGALPIRALMARNGKVDWERVDEVIYGCANQ 60

Query: 60  AGL-GQNVARQCMINAGIPKEVTAFTINKVCGSGLRAVSLAAQVIKAGDADIIMAGGTEN 118
           AG   +NVAR   + AG+P  V   TIN++CGSG+ AV  AA+ IK G+  +++AGG E+
Sbjct: 61  AGEDNRNVARMAGLLAGLPVAVAGATINRLCGSGMDAVGTAARAIKTGETALMIAGGVES 120

Query: 119 MDKAPFILPNARWGYRMSMPKGDLIDEMVWGGLTDVFNGYH----MGITAENINDMYGIT 174
           M +APF++P A   +  S    D    + W  +  +    +    M  TA+N+   + I 
Sbjct: 121 MSRAPFVMPKADSAFSRSNAVYDTT--IGWRFVNKLMKQQYGVDSMPETADNVAADFCIG 178

Query: 175 REEQDAFGFRSQTLAAQAIESGRFKDEIVPVVIKGKKGDI-VFDTDEHPRKSTP-EAMAK 232
           R EQDAF  RSQ   A A   G FKDEI PV I  KKG+  +FDTDEHPR  T  E +AK
Sbjct: 179 RAEQDAFALRSQQRWAAAQAKGLFKDEIAPVEIAQKKGESKIFDTDEHPRPDTTLEQLAK 238

Query: 233 LAPAFKKGGSVTAGNASGINDAAAAVIVMSKEKADELGIKPMAKVVSYASGGVDPSVMGL 292
           L        +VTAGNASG+ND A A+++ S+  A   G+ P A+VV+ A+ GV P +MG 
Sbjct: 239 LKGINGPDLTVTAGNASGVNDGACALLLASEAAAKAHGLTPRARVVAMATAGVAPRIMGF 298

Query: 293 GPIPASRKALEKAGLTIDDIDLIEANEAFAAQSIAVARDLGWADKMEKVNVNGGAIAIGH 352
           GP PA +K L   GL ++ +D+IE NEAFAAQ +AV RDLG AD   +VN  GGAIAIGH
Sbjct: 299 GPAPAVKKLLALTGLRLEQMDVIELNEAFAAQGLAVTRDLGLADDDARVNPYGGAIAIGH 358

Query: 353 PIGSSGARILVTLLYEMQKRGSKKGLATLCIGGGMGTALIVE 394
           P+G SGAR++ T +Y++ + G +  L T+CIG G G A+++E
Sbjct: 359 PLGMSGARLVTTAMYQLHRTGGRYALCTMCIGVGQGIAMVIE 400


Lambda     K      H
   0.317    0.135    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: 447
Number of extensions: 24
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: 396
Length of database: 402
Length adjustment: 31
Effective length of query: 365
Effective length of database: 371
Effective search space:   135415
Effective search space used:   135415
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.3 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 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