Source | Evidence on protein | Close homologs |
---|---|---|
Cuervo et al. | no | yes: 0 |
Hassani et al. | no | yes: 0 |
Forrest at al. (metacyclic) | no | yes: 0 |
Forrest at al. (procyclic) | no | yes: 0 |
Silverman et al. | no | yes: 0 |
Pissara et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Pires et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Silverman et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Jamdhade et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 9 |
NetGPI | no | yes: 0, no: 9 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005815 | microtubule organizing center | 2 | 1 |
GO:0005874 | microtubule | 6 | 1 |
GO:0005881 | cytoplasmic microtubule | 7 | 1 |
GO:0035371 | microtubule plus-end | 3 | 1 |
GO:0051233 | spindle midzone | 2 | 1 |
GO:0099080 | supramolecular complex | 2 | 1 |
GO:0099081 | supramolecular polymer | 3 | 1 |
GO:0099512 | supramolecular fiber | 4 | 1 |
GO:0099513 | polymeric cytoskeletal fiber | 5 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
GO:1990752 | microtubule end | 2 | 1 |
Related structures:
AlphaFold database: A0A3S7WXV0
Term | Name | Level | Count |
---|---|---|---|
GO:0000226 | microtubule cytoskeleton organization | 3 | 1 |
GO:0006996 | organelle organization | 4 | 1 |
GO:0007010 | cytoskeleton organization | 5 | 1 |
GO:0007017 | microtubule-based process | 2 | 1 |
GO:0007051 | spindle organization | 3 | 1 |
GO:0008104 | protein localization | 4 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0016043 | cellular component organization | 3 | 1 |
GO:0022402 | cell cycle process | 2 | 1 |
GO:0022607 | cellular component assembly | 4 | 1 |
GO:0031110 | regulation of microtubule polymerization or depolymerization | 6 | 1 |
GO:0032886 | regulation of microtubule-based process | 4 | 1 |
GO:0033036 | macromolecule localization | 2 | 1 |
GO:0033043 | regulation of organelle organization | 5 | 1 |
GO:0033365 | protein localization to organelle | 5 | 1 |
GO:0035372 | protein localization to microtubule | 8 | 1 |
GO:0044380 | protein localization to cytoskeleton | 6 | 1 |
GO:0050789 | regulation of biological process | 2 | 1 |
GO:0050794 | regulation of cellular process | 3 | 1 |
GO:0051128 | regulation of cellular component organization | 4 | 1 |
GO:0051179 | localization | 1 | 1 |
GO:0051225 | spindle assembly | 4 | 1 |
GO:0051493 | regulation of cytoskeleton organization | 6 | 1 |
GO:0051641 | cellular localization | 2 | 1 |
GO:0065007 | biological regulation | 1 | 1 |
GO:0070507 | regulation of microtubule cytoskeleton organization | 5 | 1 |
GO:0070727 | cellular macromolecule localization | 3 | 1 |
GO:0070925 | organelle assembly | 5 | 1 |
GO:0071840 | cellular component organization or biogenesis | 2 | 1 |
GO:0072698 | protein localization to microtubule cytoskeleton | 7 | 1 |
GO:0140694 | non-membrane-bounded organelle assembly | 6 | 1 |
GO:1904825 | protein localization to microtubule plus-end | 10 | 1 |
GO:1905725 | protein localization to microtubule end | 9 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005488 | binding | 1 | 9 |
GO:0005515 | protein binding | 2 | 9 |
GO:0008017 | microtubule binding | 5 | 9 |
GO:0008092 | cytoskeletal protein binding | 3 | 9 |
GO:0015631 | tubulin binding | 4 | 9 |
GO:0051010 | microtubule plus-end binding | 6 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 240 | 244 | PF00656 | 0.656 |
CLV_C14_Caspase3-7 | 31 | 35 | PF00656 | 0.318 |
CLV_NRD_NRD_1 | 10 | 12 | PF00675 | 0.545 |
CLV_PCSK_SKI1_1 | 12 | 16 | PF00082 | 0.492 |
CLV_PCSK_SKI1_1 | 130 | 134 | PF00082 | 0.477 |
CLV_PCSK_SKI1_1 | 159 | 163 | PF00082 | 0.512 |
CLV_PCSK_SKI1_1 | 342 | 346 | PF00082 | 0.586 |
CLV_Separin_Metazoa | 304 | 308 | PF03568 | 0.706 |
DEG_APCC_DBOX_1 | 326 | 334 | PF00400 | 0.525 |
DEG_COP1_1 | 316 | 325 | PF00400 | 0.509 |
DEG_SCF_FBW7_1 | 251 | 258 | PF00400 | 0.596 |
DEG_SPOP_SBC_1 | 265 | 269 | PF00917 | 0.667 |
DOC_CKS1_1 | 252 | 257 | PF01111 | 0.752 |
DOC_CYCLIN_RxL_1 | 139 | 151 | PF00134 | 0.500 |
DOC_PP1_RVXF_1 | 75 | 81 | PF00149 | 0.371 |
DOC_PP1_RVXF_1 | 98 | 105 | PF00149 | 0.438 |
DOC_PP4_FxxP_1 | 252 | 255 | PF00568 | 0.716 |
DOC_USP7_MATH_1 | 189 | 193 | PF00917 | 0.537 |
DOC_USP7_MATH_1 | 245 | 249 | PF00917 | 0.691 |
DOC_USP7_MATH_1 | 255 | 259 | PF00917 | 0.771 |
DOC_USP7_MATH_1 | 265 | 269 | PF00917 | 0.602 |
DOC_USP7_MATH_1 | 28 | 32 | PF00917 | 0.421 |
DOC_USP7_MATH_1 | 418 | 422 | PF00917 | 0.541 |
DOC_USP7_MATH_1 | 55 | 59 | PF00917 | 0.553 |
DOC_USP7_MATH_1 | 90 | 94 | PF00917 | 0.586 |
DOC_USP7_UBL2_3 | 160 | 164 | PF12436 | 0.579 |
DOC_WW_Pin1_4 | 215 | 220 | PF00397 | 0.775 |
DOC_WW_Pin1_4 | 224 | 229 | PF00397 | 0.713 |
DOC_WW_Pin1_4 | 247 | 252 | PF00397 | 0.750 |
DOC_WW_Pin1_4 | 285 | 290 | PF00397 | 0.796 |
LIG_14-3-3_CanoR_1 | 123 | 127 | PF00244 | 0.533 |
LIG_14-3-3_CanoR_1 | 327 | 331 | PF00244 | 0.641 |
LIG_14-3-3_CanoR_1 | 366 | 371 | PF00244 | 0.664 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.644 |
LIG_FHA_1 | 131 | 137 | PF00498 | 0.449 |
LIG_FHA_1 | 179 | 185 | PF00498 | 0.656 |
LIG_FHA_1 | 317 | 323 | PF00498 | 0.637 |
LIG_FHA_1 | 362 | 368 | PF00498 | 0.503 |
LIG_FHA_1 | 386 | 392 | PF00498 | 0.581 |
LIG_FHA_1 | 414 | 420 | PF00498 | 0.464 |
LIG_FHA_1 | 81 | 87 | PF00498 | 0.488 |
LIG_FHA_2 | 38 | 44 | PF00498 | 0.364 |
LIG_Integrin_RGD_1 | 241 | 243 | PF01839 | 0.640 |
LIG_LIR_Apic_2 | 250 | 255 | PF02991 | 0.707 |
LIG_LIR_Gen_1 | 101 | 110 | PF02991 | 0.368 |
LIG_LIR_Nem_3 | 23 | 29 | PF02991 | 0.399 |
LIG_LYPXL_yS_3 | 26 | 29 | PF13949 | 0.350 |
LIG_NRBOX | 393 | 399 | PF00104 | 0.475 |
LIG_NRBOX | 435 | 441 | PF00104 | 0.533 |
LIG_PCNA_PIPBox_1 | 150 | 159 | PF02747 | 0.343 |
LIG_Pex14_1 | 145 | 149 | PF04695 | 0.363 |
LIG_SH2_CRK | 38 | 42 | PF00017 | 0.331 |
LIG_SH2_GRB2like | 204 | 207 | PF00017 | 0.702 |
LIG_SH2_NCK_1 | 408 | 412 | PF00017 | 0.503 |
LIG_SH2_STAP1 | 157 | 161 | PF00017 | 0.451 |
LIG_SH2_STAT5 | 147 | 150 | PF00017 | 0.464 |
LIG_SH2_STAT5 | 297 | 300 | PF00017 | 0.811 |
LIG_SH2_STAT5 | 315 | 318 | PF00017 | 0.540 |
LIG_SH2_STAT5 | 38 | 41 | PF00017 | 0.334 |
LIG_SH2_STAT5 | 74 | 77 | PF00017 | 0.479 |
LIG_SH3_3 | 425 | 431 | PF00018 | 0.553 |
LIG_SUMO_SIM_anti_2 | 138 | 144 | PF11976 | 0.402 |
LIG_SUMO_SIM_anti_2 | 435 | 441 | PF11976 | 0.509 |
LIG_SUMO_SIM_par_1 | 318 | 324 | PF11976 | 0.571 |
LIG_SUMO_SIM_par_1 | 387 | 393 | PF11976 | 0.517 |
LIG_TRAF2_1 | 301 | 304 | PF00917 | 0.606 |
LIG_TRAF2_1 | 390 | 393 | PF00917 | 0.597 |
LIG_UBA3_1 | 14 | 20 | PF00899 | 0.453 |
MOD_CDC14_SPxK_1 | 250 | 253 | PF00782 | 0.825 |
MOD_CDK_SPK_2 | 215 | 220 | PF00069 | 0.656 |
MOD_CDK_SPxK_1 | 247 | 253 | PF00069 | 0.739 |
MOD_CK1_1 | 2 | 8 | PF00069 | 0.622 |
MOD_CK1_1 | 229 | 235 | PF00069 | 0.769 |
MOD_CK1_1 | 281 | 287 | PF00069 | 0.743 |
MOD_CK1_1 | 421 | 427 | PF00069 | 0.604 |
MOD_CK1_1 | 93 | 99 | PF00069 | 0.410 |
MOD_CK2_1 | 229 | 235 | PF00069 | 0.783 |
MOD_CK2_1 | 298 | 304 | PF00069 | 0.671 |
MOD_CK2_1 | 357 | 363 | PF00069 | 0.610 |
MOD_CK2_1 | 37 | 43 | PF00069 | 0.446 |
MOD_CK2_1 | 377 | 383 | PF00069 | 0.594 |
MOD_CK2_1 | 387 | 393 | PF00069 | 0.592 |
MOD_CK2_1 | 95 | 101 | PF00069 | 0.422 |
MOD_Cter_Amidation | 9 | 12 | PF01082 | 0.527 |
MOD_GlcNHglycan | 1 | 4 | PF01048 | 0.614 |
MOD_GlcNHglycan | 228 | 231 | PF01048 | 0.652 |
MOD_GlcNHglycan | 243 | 246 | PF01048 | 0.712 |
MOD_GlcNHglycan | 283 | 286 | PF01048 | 0.729 |
MOD_GlcNHglycan | 300 | 303 | PF01048 | 0.797 |
MOD_GlcNHglycan | 420 | 423 | PF01048 | 0.544 |
MOD_GlcNHglycan | 79 | 83 | PF01048 | 0.481 |
MOD_GlcNHglycan | 8 | 11 | PF01048 | 0.432 |
MOD_GSK3_1 | 183 | 190 | PF00069 | 0.643 |
MOD_GSK3_1 | 2 | 9 | PF00069 | 0.566 |
MOD_GSK3_1 | 224 | 231 | PF00069 | 0.654 |
MOD_GSK3_1 | 241 | 248 | PF00069 | 0.604 |
MOD_GSK3_1 | 251 | 258 | PF00069 | 0.717 |
MOD_GSK3_1 | 276 | 283 | PF00069 | 0.705 |
MOD_GSK3_1 | 353 | 360 | PF00069 | 0.592 |
MOD_N-GLC_1 | 178 | 183 | PF02516 | 0.629 |
MOD_N-GLC_1 | 214 | 219 | PF02516 | 0.637 |
MOD_NEK2_1 | 148 | 153 | PF00069 | 0.452 |
MOD_NEK2_1 | 178 | 183 | PF00069 | 0.600 |
MOD_NEK2_1 | 326 | 331 | PF00069 | 0.527 |
MOD_NEK2_1 | 78 | 83 | PF00069 | 0.449 |
MOD_NEK2_2 | 28 | 33 | PF00069 | 0.419 |
MOD_PIKK_1 | 421 | 427 | PF00454 | 0.559 |
MOD_PIKK_1 | 53 | 59 | PF00454 | 0.618 |
MOD_PK_1 | 366 | 372 | PF00069 | 0.728 |
MOD_PKA_2 | 122 | 128 | PF00069 | 0.525 |
MOD_PKA_2 | 245 | 251 | PF00069 | 0.818 |
MOD_PKA_2 | 316 | 322 | PF00069 | 0.624 |
MOD_PKA_2 | 326 | 332 | PF00069 | 0.558 |
MOD_PKA_2 | 357 | 363 | PF00069 | 0.722 |
MOD_PKA_2 | 385 | 391 | PF00069 | 0.618 |
MOD_PKA_2 | 93 | 99 | PF00069 | 0.582 |
MOD_PKB_1 | 185 | 193 | PF00069 | 0.654 |
MOD_PKB_1 | 239 | 247 | PF00069 | 0.725 |
MOD_Plk_1 | 178 | 184 | PF00069 | 0.638 |
MOD_Plk_1 | 307 | 313 | PF00069 | 0.682 |
MOD_Plk_1 | 377 | 383 | PF00069 | 0.644 |
MOD_Plk_2-3 | 387 | 393 | PF00069 | 0.599 |
MOD_Plk_2-3 | 95 | 101 | PF00069 | 0.479 |
MOD_Plk_4 | 326 | 332 | PF00069 | 0.484 |
MOD_Plk_4 | 37 | 43 | PF00069 | 0.333 |
MOD_ProDKin_1 | 215 | 221 | PF00069 | 0.780 |
MOD_ProDKin_1 | 224 | 230 | PF00069 | 0.712 |
MOD_ProDKin_1 | 247 | 253 | PF00069 | 0.754 |
MOD_ProDKin_1 | 285 | 291 | PF00069 | 0.798 |
MOD_SUMO_rev_2 | 158 | 166 | PF00179 | 0.557 |
TRG_DiLeu_BaEn_1 | 393 | 398 | PF01217 | 0.509 |
TRG_DiLeu_BaEn_4 | 399 | 405 | PF01217 | 0.456 |
TRG_DiLeu_BaLyEn_6 | 105 | 110 | PF01217 | 0.425 |
TRG_DiLeu_BaLyEn_6 | 428 | 433 | PF01217 | 0.560 |
TRG_ENDOCYTIC_2 | 147 | 150 | PF00928 | 0.434 |
TRG_ENDOCYTIC_2 | 26 | 29 | PF00928 | 0.350 |
TRG_ENDOCYTIC_2 | 38 | 41 | PF00928 | 0.334 |
TRG_ENDOCYTIC_2 | 408 | 411 | PF00928 | 0.534 |
TRG_ER_diArg_1 | 182 | 185 | PF00400 | 0.701 |
TRG_Pf-PMV_PEXEL_1 | 108 | 112 | PF00026 | 0.389 |
TRG_Pf-PMV_PEXEL_1 | 198 | 202 | PF00026 | 0.656 |
TRG_Pf-PMV_PEXEL_1 | 434 | 438 | PF00026 | 0.524 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PBZ6 | Leptomonas seymouri | 54% | 100% |
A0A1X0NWV1 | Trypanosomatidae | 34% | 100% |
A0A3R7KIS5 | Trypanosoma rangeli | 37% | 100% |
A4HCY2 | Leishmania braziliensis | 81% | 100% |
A4I0G7 | Leishmania infantum | 100% | 100% |
C9ZV68 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 32% | 100% |
E9AWC9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 93% | 100% |
Q4QB43 | Leishmania major | 93% | 100% |