Align mannose-1-phosphate guanylyltransferase (EC 2.7.7.13) (characterized)
to candidate GFF1892 PS417_09635 mannose-1-phosphate guanylyltransferase
Query= BRENDA::P07874 (481 letters) >FitnessBrowser__WCS417:GFF1892 Length = 486 Score = 412 bits (1060), Expect = e-119 Identities = 211/476 (44%), Positives = 306/476 (64%), Gaps = 11/476 (2%) Query: 1 MIPVILSGGSGSRLWPLSRKQYPKQFLALTGDDTLFQQTIKRLA-FDGMQAPLLVCNKEH 59 +IP I+SGGSG+RLWP+SR+ PK F+ + +L Q+T +R A G+++ L V N++ Sbjct: 7 LIPCIISGGSGTRLWPVSRQNMPKPFMRMRDGQSLLQKTFQRAAKLPGVESVLTVTNRDL 66 Query: 60 RFIVQEQLEAQNLASQAI--LLEPFGRNTAPAVAIAAMKLVAE-GRDELLLILPADHVIE 116 F + N A + LLEPFGRNTA A+A+AA+ + G + LL++PADH+I Sbjct: 67 LFRTLDDYRLVNKAHLPLDLLLEPFGRNTAAAIAVAALHVQEHFGGEAQLLVMPADHLIL 126 Query: 117 DQRAFQQALALATNAAEKGEMVLFGIPASRPETGYGYIRASADAQLPEGVSRVQSFVEKP 176 ++ AF +A+ A + AE G +V FGI +PETG+GYI +L G +RV+ FVEKP Sbjct: 127 NEVAFAEAVTQARDLAEAGYLVTFGIQPDQPETGFGYIEQGE--RLGTG-NRVKRFVEKP 183 Query: 177 DEARAREFVAAGGYYWNSGMFLFRASRYLEELKKHDADIYDTCLLALERSQHDGDLVN-- 234 D A A+ ++ G + WN+GMF F+AS ++EL H D+ + AL+ SQ + + Sbjct: 184 DLATAQAYLDGGKHLWNAGMFCFKASTLVDELATHAPDVLEAARAALDHSQSLQNKTSRQ 243 Query: 235 --IDAATFECCPDNSIDYAVMEKTSRACVVPLSAGWNDVGSWSSIWDVHAKDANGNVTKG 292 +D+ F PD SID A+MEK+++ VVP GW+D+GSW ++ + DA+GN G Sbjct: 244 RELDSEAFGSAPDISIDVALMEKSTQVAVVPCDIGWSDIGSWEALRQLTPSDAHGNQVNG 303 Query: 293 DVLVHDSHNCLVHGNGKLVSVIGLEDIVVVETKDAMMIAHKDRVQDVKHVVKDLDAQGRS 352 + ++HD HNC + +++ +G+ D+++V+T DA++IA R QDV+++V +L Q Sbjct: 304 EAILHDVHNCYIDSPKRVLGAVGVRDLIIVDTPDALLIADAHRSQDVRYIVAELKRQNHP 363 Query: 353 ETQNHCEVYRPWGSYDSVDMGGRFQVKHITVKPGARLSLQMHHHRAEHWIVVSGTAQVTC 412 H V RPWG+Y ++ RF++K I VKP A LSLQMHHHR+EHW+VVSG AQ+T Sbjct: 364 AYSLHRTVTRPWGTYTVLEESSRFKIKRIVVKPQASLSLQMHHHRSEHWVVVSGAAQITN 423 Query: 413 DDKTFLLTENQSTYIPIASVHRLANPGKIPLEIIEVQSGSYLGEDDIERLEDVYGR 468 ++ FL+ N+STYIP HRL NPG I L +IEVQSG YLGEDDI R +D+YGR Sbjct: 424 GEREFLINANESTYIPAGHKHRLTNPGIIDLVMIEVQSGEYLGEDDIVRFDDIYGR 479 Lambda K H 0.319 0.134 0.400 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: 594 Number of extensions: 24 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: 481 Length of database: 486 Length adjustment: 34 Effective length of query: 447 Effective length of database: 452 Effective search space: 202044 Effective search space used: 202044 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 (21.8 bits) S2: 52 (24.6 bits)
This GapMind analysis is from Apr 09 2024. The underlying query database was built on Sep 17 2021.
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:
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