GapMind for Amino acid biosynthesis

 

Alignments for a candidate for cimA in Methanococcus maripaludis C5

Align (R)-citramalate synthase (EC 2.3.3.21) (characterized)
to candidate WP_011869267.1 MMARC5_RS07725 homocitrate synthase

Query= BRENDA::Q58787
         (491 letters)



>NCBI__GCF_000016125.1:WP_011869267.1
          Length = 386

 Score =  362 bits (930), Expect = e-104
 Identities = 185/365 (50%), Positives = 250/365 (68%), Gaps = 1/365 (0%)

Query: 5   IFDTTLRDGEQTPGVSLTPNDKLEIAKKLDELGVDVIEAGSAITSKGEREGIKLITKEGL 64
           ++DTTLRDGEQTPGV  T + KLEIAKKLDEL +  IEAG  I S+ ER+ IK IT EGL
Sbjct: 20  LYDTTLRDGEQTPGVCFTHDQKLEIAKKLDELKIKQIEAGFPIVSENERKAIKSITGEGL 79

Query: 65  NAEICSFVRALPVDIDAALECDVDSVHLVVPTSPIHMKYKLRKTEDEVLETALKAVEYAK 124
           NA+I +  R L  DID A+ECDVD +   +  SP+H+KYKL K+ DEV E  +KAVEYAK
Sbjct: 80  NAQILALSRVLKEDIDKAIECDVDGIITFIAASPMHLKYKLHKSLDEVEEMGMKAVEYAK 139

Query: 125 EHGLIVELSAEDATRSDVNFLIKLFNEGEKVGADRVCVCDTVGVLTPQKSQELFKKITEN 184
           +HGL V  SAEDATR+ V  LI++    E+ GA+RV + DT+G  TPQ    +  +++ N
Sbjct: 140 DHGLFVAFSAEDATRTPVEDLIRIHKNAEEHGANRVHIADTLGCATPQAMYHICSELSSN 199

Query: 185 V-NLPVSVHCHNDFGMATANTCSAVLGGAVQCHVTVNGIGERAGNASLEEVVAALKILYG 243
           +    + VHCHNDFG A  N+   ++GGA     TVNGIGERAGNA++EE+V ALK+LY 
Sbjct: 200 LKKAHIGVHCHNDFGFAVINSIYGLIGGAKAVSTTVNGIGERAGNAAIEEIVMALKVLYD 259

Query: 244 YDTKIKMEKLYEVSRIVSRLMKLPVPPNKAIVGDNAFAHEAGIHVDGLIKNTETYEPIKP 303
           +D  +  E L E+S++V    K+ +P NK +VG+ AF HE+GIHVD +++N  TYEP  P
Sbjct: 260 HDMGLNTEILTEISKLVENYSKIRIPENKPLVGEMAFYHESGIHVDAVLENPLTYEPFLP 319

Query: 304 EMVGNRRRIILGKHSGRKALKYKLDLMGINVSDEQLNKIYERVKEFGDLGKYISDADLLA 363
           E +G +R+IILGKHSG +A+ ++L  +G+  S E+L +I ++ KE  + G  ISD     
Sbjct: 320 EKIGQKRKIILGKHSGCRAVAHRLQELGLEASREELWEIVKKTKETREEGTEISDEVFKN 379

Query: 364 IVREV 368
           IV ++
Sbjct: 380 IVDKI 384


Lambda     K      H
   0.316    0.136    0.373 

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: 521
Number of extensions: 22
Number of successful extensions: 2
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: 491
Length of database: 386
Length adjustment: 32
Effective length of query: 459
Effective length of database: 354
Effective search space:   162486
Effective search space used:   162486
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 (21.6 bits)
S2: 51 (24.3 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