Align Inositol transport system ATP-binding protein (characterized)
to candidate Pf1N1B4_4286 Inositol transport system ATP-binding protein
Query= reanno::Phaeo:GFF717 (261 letters) >FitnessBrowser__pseudo1_N1B4:Pf1N1B4_4286 Length = 526 Score = 169 bits (429), Expect = 8e-47 Identities = 88/247 (35%), Positives = 150/247 (60%), Gaps = 5/247 (2%) Query: 7 LIRMQGIEKHFGSVIALAGVSVDVFPGECHCLLGDNGAGKSTFIKTMSGVHKPTKGDILF 66 L+ + + K F V+AL+ V + V PG L+G+NGAGKST +K ++G+++P G++ Sbjct: 32 LLEIINVSKGFPGVVALSDVQLRVRPGSVLALMGENGAGKSTLMKIIAGIYQPDAGELRL 91 Query: 67 EGQPLHFADPRDAIAAGIATVHQHLAMIPLMSVSRNFFMGNEPIRKIGPLKLFDHDYANR 126 G+P+ F P A+ AGIA +HQ L ++P MS++ N ++G E ++ L + DH +R Sbjct: 92 RGKPVVFETPLAALQAGIAMIHQELNLMPHMSIAENIWIGRE---QLNGLHMIDHREMHR 148 Query: 127 ITMEEMRKMGINLRGPDQAVGTLSGGERQTVAIARAVHFGAKVLILDEPTSALGVRQTAN 186 T + + ++ INL P++ VG LS ERQ V IA+AV + + +LI+DEPTSA+ ++ A+ Sbjct: 149 CTAKLLERLRINL-DPEELVGNLSIAERQMVEIAKAVSYDSDILIMDEPTSAITDKEVAH 207 Query: 187 VLATIDKVRKQGVAVVFITHNVRHALAVGDRFTVLNRGKTLGTAQRGDISAEELQDMMAG 246 + + I +++QG +++ITH + ++ D V G +G + + + L MM Sbjct: 208 LFSIIADLKRQGKGIIYITHKMNEVFSIADEVAVFRDGAYIGLQRADSMDGDSLISMMV- 266 Query: 247 GQELATL 253 G+EL+ L Sbjct: 267 GRELSQL 273 Score = 97.4 bits (241), Expect = 5e-25 Identities = 64/225 (28%), Positives = 110/225 (48%), Gaps = 7/225 (3%) Query: 26 VSVDVFPGECHCLLGDNGAGKSTFIKTMSGVHKPTKGDILFEGQPLHFADPRDAIAAGIA 85 VS D+ GE + G G+G++ + + G+ G+I +G+ + +DP AI G A Sbjct: 300 VSFDLHAGEILGIAGLMGSGRTNVAEAIFGITPSDGGEIRLDGEVVRISDPHMAIEKGFA 359 Query: 86 TVHQHL---AMIPLMSVSRNFFMGNEPIRKIGPLKLFDHDYANRITMEEM-RKMGINLRG 141 + + + P +SV N M P +G F A R E+M +K+ + Sbjct: 360 LLTEDRKLSGLFPCLSVLENMEMAVLP-HYVG--NGFIQQKALRALCEDMCKKLRVKTPS 416 Query: 142 PDQAVGTLSGGERQTVAIARAVHFGAKVLILDEPTSALGVRQTANVLATIDKVRKQGVAV 201 +Q + TLSGG +Q +AR + ++LILDEPT + V A + I + +G+AV Sbjct: 417 LEQCIDTLSGGNQQKALLARWLMTNPRILILDEPTRGIDVGAKAEIYRLISYLASEGMAV 476 Query: 202 VFITHNVRHALAVGDRFTVLNRGKTLGTAQRGDISAEELQDMMAG 246 + I+ + L + DR V++ G +GT R + + E + + +G Sbjct: 477 IMISSELPEVLGMSDRVMVMHEGDLMGTLDRSEATQERVMQLASG 521 Lambda K H 0.321 0.137 0.395 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: 307 Number of extensions: 22 Number of successful extensions: 4 Number of sequences better than 1.0e-02: 1 Number of HSP's gapped: 2 Number of HSP's successfully gapped: 2 Length of query: 261 Length of database: 526 Length adjustment: 30 Effective length of query: 231 Effective length of database: 496 Effective search space: 114576 Effective search space used: 114576 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: 49 (23.5 bits)
This GapMind analysis is from Sep 17 2021. 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