GapMind for Amino acid biosynthesis

 

Alignments for a candidate for metC in Sphingomonas wittichii RW1

Align alanine racemase (EC 5.1.1.1) (characterized)
to candidate WP_012049960.1 SWIT_RS19075 cystathionine beta-lyase

Query= BRENDA::P06721
         (395 letters)



>NCBI__GCF_000016765.1:WP_012049960.1
          Length = 398

 Score =  362 bits (929), Expect = e-104
 Identities = 197/390 (50%), Positives = 255/390 (65%), Gaps = 8/390 (2%)

Query: 5   KLDTQLVNAGRSKKYTLGAVNSVIQRASSLVFDSVEAKKHATRNRANGELFYGRRGTLTH 64
           K  T+LV AGR  K   G VN  + RAS+++FDSV   +   R   +G L+YGRRGT T 
Sbjct: 10  KPGTRLVTAGRHAKNRRGIVNPPVWRASTILFDSVAELRAGVRKPDDG-LYYGRRGTPTQ 68

Query: 65  FSLQQAMCELE-GGAGCVLFPCGAAAVANSILAFIEQGDHVLMTNTAYEPSQDFCSKILS 123
           +SL +A+ ELE G AG VL+P G AA++  +L+ +  GD +LM ++AYEPS+  C+ +L 
Sbjct: 69  WSLAEALTELEPGAAGTVLYPSGVAAISAVLLSLLAPGDELLMVDSAYEPSRAICNGLLR 128

Query: 124 KLGVTTSWFDPLIGADIVKHLQPNTKIVFLESPGSITMEVHDVPAIVAAVRSVVPDAIIM 183
           + G+ T ++DP IGA I   +   T++VFLESPGS+T EV DVPAI AA R+       +
Sbjct: 129 RFGIETRFYDPAIGAGIADLIGDRTRVVFLESPGSLTFEVQDVPAIAAAARA--RGVTTV 186

Query: 184 IDNTWAAGVLFKALDFGIDVSIQAATKYLVGHSDAMIGTAVCNARCWEQLRENAYLMGQM 243
           +DNTWA  +LF AL  G+D+SI A TKY+VGHSD M+G+A      +E+LR  ++ +GQ 
Sbjct: 187 LDNTWATPLLFPALAHGVDISILACTKYIVGHSDVMMGSATAVPGHFEKLRRTSHALGQC 246

Query: 244 VDADTAYITSRGLRTLGVRLRQHHESSLKVAEWLAEHPQVARVNHPALPGSKGHEFWKRD 303
           V  D AY+ +RGLRTL +RLRQH E +L VA WLAE PQVARV HPALP   GHE WKRD
Sbjct: 247 VSPDDAYLAARGLRTLQLRLRQHEEGALAVARWLAEQPQVARVLHPALPDCPGHELWKRD 306

Query: 304 FTGSSGLFSFVLKKKLNNEELANYLDNFSLFSMAYSWGGYESLILANQPEHIAAIRPQGE 363
           F+G+SGLFS VL    ++   A  +D   LF + +SWGGYESL L   P   A +R    
Sbjct: 307 FSGASGLFSIVLDGG-DDAARAALIDGLDLFGIGFSWGGYESLALPVDP---AGLRTATS 362

Query: 364 IDFSGTLIRLHIGLEDVDDLIADLDAGFAR 393
               G  IRLHIG+ED  DLIADL  G AR
Sbjct: 363 WQAEGPAIRLHIGIEDPADLIADLGRGLAR 392


Lambda     K      H
   0.321    0.135    0.402 

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: 455
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: 395
Length of database: 398
Length adjustment: 31
Effective length of query: 364
Effective length of database: 367
Effective search space:   133588
Effective search space used:   133588
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 Apr 10 2024. The underlying query database was built on Apr 09 2024.

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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