Align Inositol transport ATP-binding protein IatA, component of The myoinositol (high affinity)/ D-ribose (low affinity) transporter IatP/IatA/IbpA. The structure of IbpA with myoinositol bound has been solved (characterized)
to candidate AZOBR_RS31245 AZOBR_RS31245 ABC transporter ATP-binding protein
Query= TCDB::B8H229 (515 letters) >FitnessBrowser__azobra:AZOBR_RS31245 Length = 518 Score = 350 bits (898), Expect = e-101 Identities = 203/509 (39%), Positives = 313/509 (61%), Gaps = 11/509 (2%) Query: 1 MTLLDVSQVSKSFPGVRALDQVDLVVGVGEVHALLGENGAGKSTLIKILSAAHAADA--G 58 M +L++ ++K+FPGV+ALD V+L V GE+HAL+GENGAGKSTL+K+LS + + G Sbjct: 3 MPILEMKGITKTFPGVKALDDVNLSVREGEIHALIGENGAGKSTLMKVLSGVYPQGSFDG 62 Query: 59 TVTFAGQVLDPRDAPLRRQQLGIATIYQEFNLFPELSVAENMYLGREPRRLGLVDWSRLR 118 + F GQ R ++LGI I+QE L P LS+ EN++LG E G++DW Sbjct: 63 EIRFRGQPQAFRGIA-DSERLGIIIIHQELALVPLLSITENLFLGNEQASRGVIDWDAAT 121 Query: 119 ADAQALLNDLGLPLNPDAPVRGLTVAEQQMVEIAKAMTLNARLIIMDEPTAALSGREVDR 178 A+ LL +GL P+ + + V +QQ+VEIAKA++ +L+I+DEPTA+L+ + D Sbjct: 122 LRARELLRLVGLHDPPETLITDIGVGKQQLVEIAKALSKEVKLLILDEPTASLNESDSDA 181 Query: 179 LHAIIAGLKARSVSVIYVSHRLGEVKAMCDRYTVMRDGRFVASGDVADVEVAD--MVRLM 236 L ++ KAR ++ I +SH+L E+ + DR T++RDG V + D + V+ ++R M Sbjct: 182 LLELLLQFKARGIASILISHKLNEIAKVADRVTILRDGTTVETLDCREAVVSQDRIIRGM 241 Query: 237 VGRHVEFERRKRRRPPGAVVLKVEGVTPAAPRLSAPGYLRQVSFAARGGEIVGLAGLVGA 296 VGR + +R PG V+ +V+G + P +R V+ R GE+VG+AGL+GA Sbjct: 242 VGRALSDRYPRRTTVPGDVLFEVKGWSADHPAHPGRRVVRDVNLTVRRGEVVGIAGLMGA 301 Query: 297 GRTDLARLIFGAD--PIAAGRVLVDDKPLRLRSPRDAIQAGIMLVPEDRKQQGCFLDHSI 354 GRT+ A +FG G+ +D + + + + A+ G+ EDRK G LD+ I Sbjct: 302 GRTEFAMSLFGRSYGRNIRGQAFLDGREIDVSTISRAMANGLAYATEDRKHLGLVLDNDI 361 Query: 355 RRNLSLPSLKALSALGQWV-DERAERDLVETYRQKLRIKMADAETAIGKLSGGNQQKVLL 413 R N++L +L+ ++ +WV D E + E +R++LRI+ AD LSGGNQQKV+L Sbjct: 362 RHNVTLANLRGVAK--RWVIDHEREVQVAEEFRRRLRIRCADVFQETVNLSGGNQQKVVL 419 Query: 414 GRAMALTPKVLIVDEPTRGIDIGAKAEVHQVLSDLADLGVAVVVISSELAEVMAVSDRIV 473 + + P+VLI+DEPTRGID+GAK E++ +++ L G VV+ISSE+ E++ V+DRI Sbjct: 420 SKWLFADPQVLILDEPTRGIDVGAKYEIYTIINQLVAEGRGVVLISSEMPELLGVADRIY 479 Query: 474 VFREGVIVADLDAQTATEEGLM-AYMATG 501 V G +VA++ A A++E +M A M +G Sbjct: 480 VMNAGEMVAEMPAAEASQEKIMGAIMRSG 508 Lambda K H 0.320 0.136 0.380 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: 699 Number of extensions: 37 Number of successful extensions: 9 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: 515 Length of database: 518 Length adjustment: 35 Effective length of query: 480 Effective length of database: 483 Effective search space: 231840 Effective search space used: 231840 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