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. | yes | yes: 25 |
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. | yes | yes: 8 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 20 |
NetGPI | no | yes: 0, no: 20 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005929 | cilium | 4 | 21 |
GO:0042995 | cell projection | 2 | 21 |
GO:0043226 | organelle | 2 | 21 |
GO:0043227 | membrane-bounded organelle | 3 | 21 |
GO:0110165 | cellular anatomical entity | 1 | 21 |
GO:0120025 | plasma membrane bounded cell projection | 3 | 21 |
GO:0005634 | nucleus | 5 | 3 |
GO:0043229 | intracellular organelle | 3 | 3 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 3 |
GO:0005643 | nuclear pore | 3 | 1 |
GO:0005737 | cytoplasm | 2 | 1 |
GO:0032991 | protein-containing complex | 1 | 1 |
GO:0140513 | nuclear protein-containing complex | 2 | 1 |
Related structures:
AlphaFold database: A0A3S7X0T0
Term | Name | Level | Count |
---|---|---|---|
GO:0006810 | transport | 3 | 3 |
GO:0015931 | nucleobase-containing compound transport | 5 | 3 |
GO:0050657 | nucleic acid transport | 6 | 3 |
GO:0050658 | RNA transport | 4 | 3 |
GO:0051028 | mRNA transport | 5 | 3 |
GO:0051179 | localization | 1 | 3 |
GO:0051234 | establishment of localization | 2 | 3 |
GO:0051236 | establishment of RNA localization | 3 | 3 |
GO:0071702 | organic substance transport | 4 | 3 |
GO:0071705 | nitrogen compound transport | 4 | 3 |
GO:0006405 | RNA export from nucleus | 5 | 2 |
GO:0006406 | mRNA export from nucleus | 6 | 2 |
GO:0006913 | nucleocytoplasmic transport | 5 | 2 |
GO:0009987 | cellular process | 1 | 2 |
GO:0016973 | poly(A)+ mRNA export from nucleus | 7 | 2 |
GO:0046907 | intracellular transport | 3 | 2 |
GO:0051168 | nuclear export | 6 | 2 |
GO:0051169 | nuclear transport | 4 | 2 |
GO:0051641 | cellular localization | 2 | 2 |
GO:0051649 | establishment of localization in cell | 3 | 2 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005488 | binding | 1 | 11 |
GO:0043167 | ion binding | 2 | 10 |
GO:0043169 | cation binding | 3 | 10 |
GO:0046872 | metal ion binding | 4 | 10 |
GO:0003676 | nucleic acid binding | 3 | 2 |
GO:0003723 | RNA binding | 4 | 2 |
GO:0097159 | organic cyclic compound binding | 2 | 2 |
GO:1901363 | heterocyclic compound binding | 2 | 2 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 482 | 484 | PF00675 | 0.560 |
CLV_PCSK_KEX2_1 | 117 | 119 | PF00082 | 0.658 |
CLV_PCSK_KEX2_1 | 191 | 193 | PF00082 | 0.529 |
CLV_PCSK_KEX2_1 | 481 | 483 | PF00082 | 0.569 |
CLV_PCSK_KEX2_1 | 532 | 534 | PF00082 | 0.549 |
CLV_PCSK_PC1ET2_1 | 117 | 119 | PF00082 | 0.658 |
CLV_PCSK_PC1ET2_1 | 191 | 193 | PF00082 | 0.578 |
CLV_PCSK_PC1ET2_1 | 532 | 534 | PF00082 | 0.520 |
CLV_PCSK_SKI1_1 | 153 | 157 | PF00082 | 0.516 |
CLV_PCSK_SKI1_1 | 169 | 173 | PF00082 | 0.465 |
CLV_PCSK_SKI1_1 | 233 | 237 | PF00082 | 0.658 |
CLV_PCSK_SKI1_1 | 429 | 433 | PF00082 | 0.466 |
CLV_PCSK_SKI1_1 | 532 | 536 | PF00082 | 0.667 |
CLV_PCSK_SKI1_1 | 79 | 83 | PF00082 | 0.519 |
CLV_Separin_Metazoa | 132 | 136 | PF03568 | 0.587 |
DOC_CYCLIN_RxL_1 | 137 | 151 | PF00134 | 0.591 |
DOC_CYCLIN_RxL_1 | 153 | 160 | PF00134 | 0.592 |
DOC_CYCLIN_RxL_1 | 76 | 83 | PF00134 | 0.621 |
DOC_CYCLIN_yClb1_LxF_4 | 181 | 187 | PF00134 | 0.584 |
DOC_CYCLIN_yCln2_LP_2 | 402 | 408 | PF00134 | 0.487 |
DOC_MAPK_DCC_7 | 215 | 225 | PF00069 | 0.673 |
DOC_MAPK_gen_1 | 135 | 144 | PF00069 | 0.509 |
DOC_MAPK_MEF2A_6 | 218 | 225 | PF00069 | 0.558 |
DOC_MAPK_MEF2A_6 | 363 | 371 | PF00069 | 0.616 |
DOC_MAPK_MEF2A_6 | 507 | 515 | PF00069 | 0.673 |
DOC_MAPK_MEF2A_6 | 79 | 86 | PF00069 | 0.594 |
DOC_MAPK_NFAT4_5 | 79 | 87 | PF00069 | 0.607 |
DOC_PP2B_LxvP_1 | 236 | 239 | PF13499 | 0.643 |
DOC_PP2B_LxvP_1 | 514 | 517 | PF13499 | 0.647 |
DOC_USP7_MATH_1 | 11 | 15 | PF00917 | 0.604 |
DOC_USP7_MATH_1 | 241 | 245 | PF00917 | 0.658 |
DOC_USP7_MATH_1 | 319 | 323 | PF00917 | 0.703 |
DOC_USP7_MATH_1 | 334 | 338 | PF00917 | 0.677 |
DOC_USP7_MATH_1 | 499 | 503 | PF00917 | 0.618 |
DOC_USP7_MATH_1 | 523 | 527 | PF00917 | 0.665 |
DOC_USP7_MATH_2 | 348 | 354 | PF00917 | 0.475 |
DOC_WW_Pin1_4 | 106 | 111 | PF00397 | 0.590 |
DOC_WW_Pin1_4 | 460 | 465 | PF00397 | 0.602 |
DOC_WW_Pin1_4 | 470 | 475 | PF00397 | 0.662 |
LIG_14-3-3_CanoR_1 | 325 | 333 | PF00244 | 0.599 |
LIG_14-3-3_CanoR_1 | 429 | 434 | PF00244 | 0.452 |
LIG_Actin_WH2_2 | 310 | 327 | PF00022 | 0.540 |
LIG_APCC_ABBAyCdc20_2 | 455 | 461 | PF00400 | 0.723 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.653 |
LIG_BRCT_BRCA1_1 | 122 | 126 | PF00533 | 0.493 |
LIG_BRCT_BRCA1_1 | 326 | 330 | PF00533 | 0.513 |
LIG_BRCT_BRCA1_1 | 423 | 427 | PF00533 | 0.518 |
LIG_BRCT_BRCA1_1 | 465 | 469 | PF00533 | 0.643 |
LIG_BRCT_BRCA1_1 | 82 | 86 | PF00533 | 0.557 |
LIG_BRCT_BRCA1_1 | 90 | 94 | PF00533 | 0.544 |
LIG_BRCT_BRCA1_2 | 122 | 128 | PF00533 | 0.512 |
LIG_BRCT_BRCA1_2 | 82 | 88 | PF00533 | 0.605 |
LIG_FHA_1 | 304 | 310 | PF00498 | 0.570 |
LIG_FHA_1 | 428 | 434 | PF00498 | 0.422 |
LIG_FHA_1 | 487 | 493 | PF00498 | 0.591 |
LIG_FHA_2 | 423 | 429 | PF00498 | 0.538 |
LIG_FHA_2 | 498 | 504 | PF00498 | 0.617 |
LIG_IRF3_LxIS_1 | 282 | 288 | PF10401 | 0.603 |
LIG_LIR_Gen_1 | 120 | 129 | PF02991 | 0.487 |
LIG_LIR_Gen_1 | 261 | 271 | PF02991 | 0.627 |
LIG_LIR_Gen_1 | 280 | 287 | PF02991 | 0.615 |
LIG_LIR_Gen_1 | 87 | 97 | PF02991 | 0.620 |
LIG_LIR_Nem_3 | 120 | 124 | PF02991 | 0.491 |
LIG_LIR_Nem_3 | 268 | 274 | PF02991 | 0.565 |
LIG_LIR_Nem_3 | 280 | 285 | PF02991 | 0.599 |
LIG_LIR_Nem_3 | 327 | 333 | PF02991 | 0.608 |
LIG_LIR_Nem_3 | 87 | 93 | PF02991 | 0.611 |
LIG_LRP6_Inhibitor_1 | 147 | 153 | PF00058 | 0.472 |
LIG_MLH1_MIPbox_1 | 423 | 427 | PF16413 | 0.546 |
LIG_MYND_1 | 110 | 114 | PF01753 | 0.545 |
LIG_NRBOX | 154 | 160 | PF00104 | 0.504 |
LIG_NRBOX | 195 | 201 | PF00104 | 0.472 |
LIG_NRBOX | 80 | 86 | PF00104 | 0.493 |
LIG_PCNA_PIPBox_1 | 251 | 260 | PF02747 | 0.577 |
LIG_Pex14_2 | 371 | 375 | PF04695 | 0.648 |
LIG_PTB_Apo_2 | 369 | 376 | PF02174 | 0.640 |
LIG_REV1ctd_RIR_1 | 424 | 433 | PF16727 | 0.477 |
LIG_SH2_CRK | 121 | 125 | PF00017 | 0.601 |
LIG_SH2_CRK | 193 | 197 | PF00017 | 0.583 |
LIG_SH2_CRK | 271 | 275 | PF00017 | 0.545 |
LIG_SH2_CRK | 90 | 94 | PF00017 | 0.600 |
LIG_SH2_NCK_1 | 121 | 125 | PF00017 | 0.601 |
LIG_SH2_NCK_1 | 271 | 275 | PF00017 | 0.447 |
LIG_SH2_NCK_1 | 90 | 94 | PF00017 | 0.576 |
LIG_SH2_SRC | 276 | 279 | PF00017 | 0.443 |
LIG_SH2_STAP1 | 212 | 216 | PF00017 | 0.490 |
LIG_SH2_STAP1 | 90 | 94 | PF00017 | 0.629 |
LIG_SH2_STAT3 | 257 | 260 | PF00017 | 0.623 |
LIG_SH2_STAT3 | 278 | 281 | PF00017 | 0.624 |
LIG_SH2_STAT5 | 257 | 260 | PF00017 | 0.541 |
LIG_SH2_STAT5 | 276 | 279 | PF00017 | 0.550 |
LIG_SH2_STAT5 | 401 | 404 | PF00017 | 0.451 |
LIG_SH3_3 | 402 | 408 | PF00018 | 0.487 |
LIG_SH3_3 | 410 | 416 | PF00018 | 0.462 |
LIG_SH3_3 | 461 | 467 | PF00018 | 0.717 |
LIG_SUMO_SIM_anti_2 | 198 | 203 | PF11976 | 0.535 |
LIG_SUMO_SIM_par_1 | 428 | 434 | PF11976 | 0.557 |
LIG_TRAF2_1 | 502 | 505 | PF00917 | 0.763 |
LIG_TYR_ITIM | 119 | 124 | PF00017 | 0.598 |
LIG_UBA3_1 | 81 | 88 | PF00899 | 0.493 |
LIG_WRC_WIRS_1 | 423 | 428 | PF05994 | 0.595 |
MOD_CDK_SPxK_1 | 470 | 476 | PF00069 | 0.703 |
MOD_CK1_1 | 185 | 191 | PF00069 | 0.548 |
MOD_CK1_1 | 265 | 271 | PF00069 | 0.582 |
MOD_CK1_1 | 280 | 286 | PF00069 | 0.577 |
MOD_CK1_1 | 337 | 343 | PF00069 | 0.674 |
MOD_CK1_1 | 69 | 75 | PF00069 | 0.660 |
MOD_CK2_1 | 472 | 478 | PF00069 | 0.521 |
MOD_CK2_1 | 498 | 504 | PF00069 | 0.647 |
MOD_CK2_1 | 523 | 529 | PF00069 | 0.611 |
MOD_Cter_Amidation | 5 | 8 | PF01082 | 0.681 |
MOD_GlcNHglycan | 15 | 18 | PF01048 | 0.775 |
MOD_GlcNHglycan | 174 | 177 | PF01048 | 0.491 |
MOD_GlcNHglycan | 187 | 190 | PF01048 | 0.491 |
MOD_GlcNHglycan | 243 | 246 | PF01048 | 0.754 |
MOD_GlcNHglycan | 282 | 285 | PF01048 | 0.577 |
MOD_GlcNHglycan | 300 | 303 | PF01048 | 0.524 |
MOD_GlcNHglycan | 336 | 339 | PF01048 | 0.744 |
MOD_GlcNHglycan | 35 | 38 | PF01048 | 0.887 |
MOD_GlcNHglycan | 63 | 66 | PF01048 | 0.750 |
MOD_GlcNHglycan | 68 | 71 | PF01048 | 0.759 |
MOD_GSK3_1 | 210 | 217 | PF00069 | 0.664 |
MOD_GSK3_1 | 241 | 248 | PF00069 | 0.667 |
MOD_GSK3_1 | 258 | 265 | PF00069 | 0.484 |
MOD_GSK3_1 | 319 | 326 | PF00069 | 0.625 |
MOD_GSK3_1 | 407 | 414 | PF00069 | 0.596 |
MOD_GSK3_1 | 427 | 434 | PF00069 | 0.473 |
MOD_GSK3_1 | 436 | 443 | PF00069 | 0.506 |
MOD_GSK3_1 | 59 | 66 | PF00069 | 0.801 |
MOD_N-GLC_1 | 101 | 106 | PF02516 | 0.536 |
MOD_N-GLC_1 | 177 | 182 | PF02516 | 0.654 |
MOD_N-GLC_1 | 497 | 502 | PF02516 | 0.641 |
MOD_N-GLC_1 | 59 | 64 | PF02516 | 0.815 |
MOD_N-GLC_1 | 66 | 71 | PF02516 | 0.760 |
MOD_N-GLC_2 | 357 | 359 | PF02516 | 0.408 |
MOD_NEK2_1 | 101 | 106 | PF00069 | 0.565 |
MOD_NEK2_1 | 258 | 263 | PF00069 | 0.514 |
MOD_NEK2_1 | 277 | 282 | PF00069 | 0.549 |
MOD_NEK2_1 | 285 | 290 | PF00069 | 0.496 |
MOD_NEK2_1 | 380 | 385 | PF00069 | 0.576 |
MOD_NEK2_1 | 422 | 427 | PF00069 | 0.462 |
MOD_NEK2_1 | 86 | 91 | PF00069 | 0.509 |
MOD_NEK2_2 | 391 | 396 | PF00069 | 0.445 |
MOD_PIKK_1 | 245 | 251 | PF00454 | 0.575 |
MOD_PIKK_1 | 277 | 283 | PF00454 | 0.654 |
MOD_PIKK_1 | 324 | 330 | PF00454 | 0.655 |
MOD_PIKK_1 | 407 | 413 | PF00454 | 0.598 |
MOD_PIKK_1 | 88 | 94 | PF00454 | 0.664 |
MOD_PK_1 | 177 | 183 | PF00069 | 0.430 |
MOD_PKA_2 | 214 | 220 | PF00069 | 0.602 |
MOD_PKA_2 | 324 | 330 | PF00069 | 0.580 |
MOD_Plk_1 | 148 | 154 | PF00069 | 0.518 |
MOD_Plk_1 | 177 | 183 | PF00069 | 0.565 |
MOD_Plk_1 | 258 | 264 | PF00069 | 0.608 |
MOD_Plk_1 | 361 | 367 | PF00069 | 0.632 |
MOD_Plk_1 | 380 | 386 | PF00069 | 0.418 |
MOD_Plk_1 | 427 | 433 | PF00069 | 0.496 |
MOD_Plk_1 | 86 | 92 | PF00069 | 0.589 |
MOD_Plk_4 | 182 | 188 | PF00069 | 0.561 |
MOD_Plk_4 | 250 | 256 | PF00069 | 0.579 |
MOD_Plk_4 | 258 | 264 | PF00069 | 0.468 |
MOD_Plk_4 | 422 | 428 | PF00069 | 0.584 |
MOD_Plk_4 | 506 | 512 | PF00069 | 0.629 |
MOD_Plk_4 | 80 | 86 | PF00069 | 0.497 |
MOD_ProDKin_1 | 106 | 112 | PF00069 | 0.583 |
MOD_ProDKin_1 | 460 | 466 | PF00069 | 0.598 |
MOD_ProDKin_1 | 470 | 476 | PF00069 | 0.655 |
MOD_SUMO_rev_2 | 501 | 509 | PF00179 | 0.676 |
TRG_DiLeu_BaEn_1 | 96 | 101 | PF01217 | 0.450 |
TRG_ENDOCYTIC_2 | 121 | 124 | PF00928 | 0.598 |
TRG_ENDOCYTIC_2 | 193 | 196 | PF00928 | 0.495 |
TRG_ENDOCYTIC_2 | 271 | 274 | PF00928 | 0.549 |
TRG_ENDOCYTIC_2 | 90 | 93 | PF00928 | 0.631 |
TRG_ER_diArg_1 | 141 | 144 | PF00400 | 0.603 |
TRG_ER_diArg_1 | 480 | 483 | PF00400 | 0.576 |
TRG_Pf-PMV_PEXEL_1 | 128 | 132 | PF00026 | 0.577 |
TRG_Pf-PMV_PEXEL_1 | 143 | 148 | PF00026 | 0.577 |
TRG_Pf-PMV_PEXEL_1 | 331 | 336 | PF00026 | 0.621 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P8E9 | Leptomonas seymouri | 24% | 86% |
A0A0N0P8S6 | Leptomonas seymouri | 75% | 100% |
A0A0S4IW66 | Bodo saltans | 28% | 100% |
A0A1X0P4A3 | Trypanosomatidae | 45% | 100% |
A0A1X0P4L1 | Trypanosomatidae | 26% | 92% |
A0A3R7NID6 | Trypanosoma rangeli | 27% | 92% |
A0A3S7X0T8 | Leishmania donovani | 25% | 87% |
A4HFU3 | Leishmania braziliensis | 87% | 100% |
A4HFU4 | Leishmania braziliensis | 26% | 100% |
A4I2W0 | Leishmania infantum | 100% | 100% |
A4I2W1 | Leishmania infantum | 25% | 100% |
D0A641 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 39% | 100% |
D0A644 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 28% | 100% |
E9ADE7 | Leishmania major | 97% | 100% |
E9ADE8 | Leishmania major | 25% | 100% |
E9AZ71 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 92% | 100% |
E9AZ72 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 25% | 100% |
V5B0W6 | Trypanosoma cruzi | 26% | 93% |
V5BQG4 | Trypanosoma cruzi | 44% | 100% |