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. | yes | yes: 9 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 10 |
NetGPI | no | yes: 0, no: 10 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005634 | nucleus | 5 | 1 |
GO:0032797 | SMN complex | 3 | 1 |
GO:0032991 | protein-containing complex | 1 | 1 |
GO:0043226 | organelle | 2 | 1 |
GO:0043227 | membrane-bounded organelle | 3 | 1 |
GO:0043229 | intracellular organelle | 3 | 1 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
GO:0120114 | Sm-like protein family complex | 2 | 1 |
Related structures:
AlphaFold database: A0A3Q8IJZ4
Term | Name | Level | Count |
---|---|---|---|
GO:0000387 | spliceosomal snRNP assembly | 7 | 9 |
GO:0009987 | cellular process | 1 | 9 |
GO:0016043 | cellular component organization | 3 | 9 |
GO:0022607 | cellular component assembly | 4 | 9 |
GO:0022618 | ribonucleoprotein complex assembly | 6 | 9 |
GO:0043933 | protein-containing complex organization | 4 | 9 |
GO:0065003 | protein-containing complex assembly | 5 | 9 |
GO:0071826 | ribonucleoprotein complex subunit organization | 5 | 9 |
GO:0071840 | cellular component organization or biogenesis | 2 | 9 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 225 | 229 | PF00656 | 0.714 |
CLV_C14_Caspase3-7 | 266 | 270 | PF00656 | 0.528 |
CLV_C14_Caspase3-7 | 354 | 358 | PF00656 | 0.704 |
CLV_C14_Caspase3-7 | 369 | 373 | PF00656 | 0.687 |
CLV_NRD_NRD_1 | 169 | 171 | PF00675 | 0.656 |
CLV_NRD_NRD_1 | 237 | 239 | PF00675 | 0.705 |
CLV_NRD_NRD_1 | 290 | 292 | PF00675 | 0.527 |
CLV_NRD_NRD_1 | 500 | 502 | PF00675 | 0.521 |
CLV_NRD_NRD_1 | 516 | 518 | PF00675 | 0.271 |
CLV_PCSK_FUR_1 | 235 | 239 | PF00082 | 0.523 |
CLV_PCSK_FUR_1 | 288 | 292 | PF00082 | 0.549 |
CLV_PCSK_KEX2_1 | 237 | 239 | PF00082 | 0.654 |
CLV_PCSK_KEX2_1 | 288 | 290 | PF00082 | 0.512 |
CLV_PCSK_KEX2_1 | 500 | 502 | PF00082 | 0.541 |
CLV_PCSK_KEX2_1 | 516 | 518 | PF00082 | 0.271 |
CLV_PCSK_KEX2_1 | 80 | 82 | PF00082 | 0.681 |
CLV_PCSK_KEX2_1 | 84 | 86 | PF00082 | 0.674 |
CLV_PCSK_PC1ET2_1 | 80 | 82 | PF00082 | 0.667 |
CLV_PCSK_PC1ET2_1 | 84 | 86 | PF00082 | 0.658 |
CLV_PCSK_PC7_1 | 284 | 290 | PF00082 | 0.568 |
CLV_PCSK_SKI1_1 | 417 | 421 | PF00082 | 0.456 |
CLV_PCSK_SKI1_1 | 490 | 494 | PF00082 | 0.579 |
CLV_PCSK_SKI1_1 | 81 | 85 | PF00082 | 0.749 |
CLV_Separin_Metazoa | 250 | 254 | PF03568 | 0.398 |
DEG_APCC_DBOX_1 | 416 | 424 | PF00400 | 0.493 |
DEG_SCF_FBW7_1 | 107 | 114 | PF00400 | 0.642 |
DEG_SIAH_1 | 141 | 149 | PF03145 | 0.774 |
DEG_SPOP_SBC_1 | 111 | 115 | PF00917 | 0.765 |
DEG_SPOP_SBC_1 | 328 | 332 | PF00917 | 0.507 |
DOC_CYCLIN_yCln2_LP_2 | 453 | 459 | PF00134 | 0.546 |
DOC_MAPK_gen_1 | 189 | 199 | PF00069 | 0.503 |
DOC_MAPK_gen_1 | 316 | 326 | PF00069 | 0.482 |
DOC_MAPK_gen_1 | 516 | 523 | PF00069 | 0.327 |
DOC_PP1_RVXF_1 | 124 | 131 | PF00149 | 0.718 |
DOC_PP2B_LxvP_1 | 453 | 456 | PF13499 | 0.545 |
DOC_PP2B_PxIxI_1 | 46 | 52 | PF00149 | 0.593 |
DOC_PP4_FxxP_1 | 425 | 428 | PF00568 | 0.500 |
DOC_USP7_MATH_1 | 100 | 104 | PF00917 | 0.780 |
DOC_USP7_MATH_1 | 111 | 115 | PF00917 | 0.591 |
DOC_USP7_MATH_1 | 329 | 333 | PF00917 | 0.451 |
DOC_USP7_MATH_1 | 337 | 341 | PF00917 | 0.390 |
DOC_USP7_MATH_1 | 39 | 43 | PF00917 | 0.699 |
DOC_USP7_MATH_1 | 83 | 87 | PF00917 | 0.764 |
DOC_USP7_MATH_2 | 119 | 125 | PF00917 | 0.691 |
DOC_USP7_UBL2_3 | 80 | 84 | PF12436 | 0.773 |
DOC_USP7_UBL2_3 | 9 | 13 | PF12436 | 0.636 |
DOC_WW_Pin1_4 | 107 | 112 | PF00397 | 0.634 |
DOC_WW_Pin1_4 | 138 | 143 | PF00397 | 0.679 |
DOC_WW_Pin1_4 | 43 | 48 | PF00397 | 0.759 |
LIG_14-3-3_CanoR_1 | 215 | 222 | PF00244 | 0.665 |
LIG_14-3-3_CanoR_1 | 319 | 326 | PF00244 | 0.578 |
LIG_14-3-3_CanoR_1 | 417 | 423 | PF00244 | 0.523 |
LIG_14-3-3_CanoR_1 | 436 | 441 | PF00244 | 0.552 |
LIG_14-3-3_CanoR_1 | 474 | 480 | PF00244 | 0.450 |
LIG_Actin_WH2_2 | 186 | 203 | PF00022 | 0.522 |
LIG_APCC_ABBAyCdc20_2 | 126 | 132 | PF00400 | 0.673 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.659 |
LIG_BIR_III_2 | 503 | 507 | PF00653 | 0.553 |
LIG_BIR_III_3 | 1 | 5 | PF00653 | 0.592 |
LIG_BRCT_BRCA1_1 | 15 | 19 | PF00533 | 0.668 |
LIG_BRCT_BRCA1_1 | 178 | 182 | PF00533 | 0.596 |
LIG_BRCT_BRCA1_1 | 331 | 335 | PF00533 | 0.483 |
LIG_FHA_1 | 123 | 129 | PF00498 | 0.748 |
LIG_FHA_1 | 141 | 147 | PF00498 | 0.518 |
LIG_FHA_1 | 435 | 441 | PF00498 | 0.538 |
LIG_FHA_1 | 44 | 50 | PF00498 | 0.746 |
LIG_FHA_1 | 459 | 465 | PF00498 | 0.516 |
LIG_FHA_1 | 487 | 493 | PF00498 | 0.599 |
LIG_FHA_1 | 523 | 529 | PF00498 | 0.347 |
LIG_FHA_1 | 55 | 61 | PF00498 | 0.647 |
LIG_FHA_2 | 365 | 371 | PF00498 | 0.744 |
LIG_FHA_2 | 385 | 391 | PF00498 | 0.678 |
LIG_FHA_2 | 508 | 514 | PF00498 | 0.483 |
LIG_LIR_Gen_1 | 195 | 204 | PF02991 | 0.503 |
LIG_LIR_Gen_1 | 421 | 428 | PF02991 | 0.423 |
LIG_LIR_LC3C_4 | 57 | 62 | PF02991 | 0.779 |
LIG_LIR_Nem_3 | 195 | 199 | PF02991 | 0.522 |
LIG_LIR_Nem_3 | 239 | 243 | PF02991 | 0.477 |
LIG_LIR_Nem_3 | 421 | 425 | PF02991 | 0.416 |
LIG_LIR_Nem_3 | 539 | 544 | PF02991 | 0.635 |
LIG_PCNA_PIPBox_1 | 416 | 425 | PF02747 | 0.524 |
LIG_PCNA_yPIPBox_3 | 416 | 424 | PF02747 | 0.525 |
LIG_Pex14_2 | 272 | 276 | PF04695 | 0.513 |
LIG_PTAP_UEV_1 | 141 | 146 | PF05743 | 0.781 |
LIG_REV1ctd_RIR_1 | 531 | 539 | PF16727 | 0.544 |
LIG_SH2_CRK | 283 | 287 | PF00017 | 0.551 |
LIG_SH2_CRK | 524 | 528 | PF00017 | 0.433 |
LIG_SH2_GRB2like | 306 | 309 | PF00017 | 0.591 |
LIG_SH2_PTP2 | 196 | 199 | PF00017 | 0.569 |
LIG_SH2_STAP1 | 524 | 528 | PF00017 | 0.424 |
LIG_SH2_STAT5 | 196 | 199 | PF00017 | 0.499 |
LIG_SH2_STAT5 | 306 | 309 | PF00017 | 0.468 |
LIG_SH2_STAT5 | 509 | 512 | PF00017 | 0.534 |
LIG_SH2_STAT5 | 524 | 527 | PF00017 | 0.393 |
LIG_SH2_STAT5 | 7 | 10 | PF00017 | 0.583 |
LIG_SH3_1 | 496 | 502 | PF00018 | 0.558 |
LIG_SH3_1 | 93 | 99 | PF00018 | 0.601 |
LIG_SH3_3 | 136 | 142 | PF00018 | 0.711 |
LIG_SH3_3 | 252 | 258 | PF00018 | 0.571 |
LIG_SH3_3 | 289 | 295 | PF00018 | 0.539 |
LIG_SH3_3 | 403 | 409 | PF00018 | 0.620 |
LIG_SH3_3 | 453 | 459 | PF00018 | 0.464 |
LIG_SH3_3 | 496 | 502 | PF00018 | 0.558 |
LIG_SH3_3 | 93 | 99 | PF00018 | 0.719 |
LIG_SUMO_SIM_anti_2 | 195 | 201 | PF11976 | 0.560 |
LIG_SUMO_SIM_anti_2 | 525 | 531 | PF11976 | 0.358 |
LIG_SUMO_SIM_anti_2 | 55 | 64 | PF11976 | 0.769 |
LIG_SUMO_SIM_par_1 | 518 | 525 | PF11976 | 0.373 |
LIG_TRAF2_1 | 166 | 169 | PF00917 | 0.642 |
LIG_TRAF2_1 | 25 | 28 | PF00917 | 0.720 |
LIG_TRAF2_1 | 388 | 391 | PF00917 | 0.755 |
LIG_WRC_WIRS_1 | 257 | 262 | PF05994 | 0.403 |
LIG_WRC_WIRS_1 | 419 | 424 | PF05994 | 0.414 |
LIG_WW_1 | 506 | 509 | PF00397 | 0.540 |
LIG_WW_3 | 316 | 320 | PF00397 | 0.407 |
MOD_CK1_1 | 214 | 220 | PF00069 | 0.553 |
MOD_CK1_1 | 274 | 280 | PF00069 | 0.463 |
MOD_CK1_1 | 327 | 333 | PF00069 | 0.428 |
MOD_CK1_1 | 356 | 362 | PF00069 | 0.696 |
MOD_CK1_1 | 373 | 379 | PF00069 | 0.769 |
MOD_CK1_1 | 486 | 492 | PF00069 | 0.584 |
MOD_CK1_1 | 53 | 59 | PF00069 | 0.736 |
MOD_CK2_1 | 163 | 169 | PF00069 | 0.621 |
MOD_CK2_1 | 241 | 247 | PF00069 | 0.541 |
MOD_CK2_1 | 364 | 370 | PF00069 | 0.755 |
MOD_CK2_1 | 384 | 390 | PF00069 | 0.680 |
MOD_CK2_1 | 429 | 435 | PF00069 | 0.637 |
MOD_Cter_Amidation | 10 | 13 | PF01082 | 0.686 |
MOD_GlcNHglycan | 225 | 228 | PF01048 | 0.705 |
MOD_GlcNHglycan | 276 | 279 | PF01048 | 0.489 |
MOD_GlcNHglycan | 326 | 329 | PF01048 | 0.449 |
MOD_GlcNHglycan | 331 | 334 | PF01048 | 0.356 |
MOD_GlcNHglycan | 372 | 375 | PF01048 | 0.680 |
MOD_GlcNHglycan | 402 | 405 | PF01048 | 0.603 |
MOD_GlcNHglycan | 450 | 453 | PF01048 | 0.426 |
MOD_GlcNHglycan | 485 | 488 | PF01048 | 0.582 |
MOD_GlcNHglycan | 57 | 60 | PF01048 | 0.705 |
MOD_GlcNHglycan | 87 | 90 | PF01048 | 0.759 |
MOD_GSK3_1 | 107 | 114 | PF00069 | 0.745 |
MOD_GSK3_1 | 117 | 124 | PF00069 | 0.718 |
MOD_GSK3_1 | 134 | 141 | PF00069 | 0.734 |
MOD_GSK3_1 | 324 | 331 | PF00069 | 0.434 |
MOD_GSK3_1 | 333 | 340 | PF00069 | 0.375 |
MOD_GSK3_1 | 362 | 369 | PF00069 | 0.763 |
MOD_GSK3_1 | 39 | 46 | PF00069 | 0.733 |
MOD_GSK3_1 | 49 | 56 | PF00069 | 0.684 |
MOD_GSK3_1 | 83 | 90 | PF00069 | 0.736 |
MOD_N-GLC_1 | 107 | 112 | PF02516 | 0.686 |
MOD_N-GLC_1 | 134 | 139 | PF02516 | 0.707 |
MOD_N-GLC_1 | 229 | 234 | PF02516 | 0.688 |
MOD_N-GLC_1 | 53 | 58 | PF02516 | 0.719 |
MOD_NEK2_1 | 134 | 139 | PF00069 | 0.707 |
MOD_NEK2_1 | 211 | 216 | PF00069 | 0.577 |
MOD_NEK2_1 | 251 | 256 | PF00069 | 0.545 |
MOD_NEK2_1 | 324 | 329 | PF00069 | 0.507 |
MOD_NEK2_1 | 335 | 340 | PF00069 | 0.417 |
MOD_NEK2_1 | 468 | 473 | PF00069 | 0.443 |
MOD_NEK2_1 | 492 | 497 | PF00069 | 0.544 |
MOD_PIKK_1 | 214 | 220 | PF00454 | 0.559 |
MOD_PK_1 | 436 | 442 | PF00069 | 0.509 |
MOD_PKA_2 | 214 | 220 | PF00069 | 0.567 |
MOD_PKA_2 | 318 | 324 | PF00069 | 0.588 |
MOD_PKA_2 | 362 | 368 | PF00069 | 0.766 |
MOD_PKA_2 | 435 | 441 | PF00069 | 0.570 |
MOD_PKB_1 | 434 | 442 | PF00069 | 0.538 |
MOD_PKB_1 | 85 | 93 | PF00069 | 0.779 |
MOD_Plk_1 | 183 | 189 | PF00069 | 0.489 |
MOD_Plk_1 | 27 | 33 | PF00069 | 0.767 |
MOD_Plk_1 | 356 | 362 | PF00069 | 0.665 |
MOD_Plk_2-3 | 351 | 357 | PF00069 | 0.632 |
MOD_Plk_4 | 102 | 108 | PF00069 | 0.697 |
MOD_Plk_4 | 176 | 182 | PF00069 | 0.554 |
MOD_Plk_4 | 27 | 33 | PF00069 | 0.761 |
MOD_Plk_4 | 418 | 424 | PF00069 | 0.397 |
MOD_Plk_4 | 522 | 528 | PF00069 | 0.349 |
MOD_ProDKin_1 | 107 | 113 | PF00069 | 0.636 |
MOD_ProDKin_1 | 138 | 144 | PF00069 | 0.677 |
MOD_ProDKin_1 | 43 | 49 | PF00069 | 0.762 |
MOD_SUMO_rev_2 | 166 | 172 | PF00179 | 0.602 |
TRG_DiLeu_BaEn_1 | 247 | 252 | PF01217 | 0.443 |
TRG_DiLeu_BaLyEn_6 | 281 | 286 | PF01217 | 0.480 |
TRG_DiLeu_BaLyEn_6 | 338 | 343 | PF01217 | 0.495 |
TRG_ENDOCYTIC_2 | 196 | 199 | PF00928 | 0.539 |
TRG_ENDOCYTIC_2 | 240 | 243 | PF00928 | 0.553 |
TRG_ENDOCYTIC_2 | 283 | 286 | PF00928 | 0.551 |
TRG_ENDOCYTIC_2 | 509 | 512 | PF00928 | 0.406 |
TRG_ENDOCYTIC_2 | 524 | 527 | PF00928 | 0.348 |
TRG_ENDOCYTIC_2 | 7 | 10 | PF00928 | 0.672 |
TRG_ER_diArg_1 | 235 | 238 | PF00400 | 0.632 |
TRG_ER_diArg_1 | 288 | 291 | PF00400 | 0.551 |
TRG_ER_diArg_1 | 378 | 381 | PF00400 | 0.778 |
TRG_ER_diArg_1 | 499 | 501 | PF00400 | 0.472 |
TRG_ER_diArg_1 | 515 | 517 | PF00400 | 0.253 |
TRG_NLS_MonoCore_2 | 77 | 82 | PF00514 | 0.701 |
TRG_NLS_MonoExtN_4 | 76 | 83 | PF00514 | 0.656 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PC77 | Leptomonas seymouri | 48% | 99% |
A0A0S4IYS2 | Bodo saltans | 27% | 100% |
A0A1X0P8B5 | Trypanosomatidae | 32% | 100% |
A0A3R7RAQ0 | Trypanosoma rangeli | 30% | 100% |
A4HNY7 | Leishmania braziliensis | 77% | 100% |
A4ICK6 | Leishmania infantum | 100% | 100% |
D0A2V6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 33% | 100% |
E9ASP9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 90% | 100% |
Q4Q1U6 | Leishmania major | 92% | 100% |