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: 6 |
NetGPI | no | yes: 0, no: 6 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005634 | nucleus | 5 | 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 |
Related structures:
AlphaFold database: A0A3Q8IDJ2
Term | Name | Level | Count |
---|---|---|---|
GO:0000491 | small nucleolar ribonucleoprotein complex assembly | 7 | 1 |
GO:0000492 | box C/D snoRNP assembly | 8 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0016043 | cellular component organization | 3 | 1 |
GO:0022607 | cellular component assembly | 4 | 1 |
GO:0022618 | ribonucleoprotein complex assembly | 6 | 1 |
GO:0043933 | protein-containing complex organization | 4 | 1 |
GO:0065003 | protein-containing complex assembly | 5 | 1 |
GO:0071826 | ribonucleoprotein complex subunit organization | 5 | 1 |
GO:0071840 | cellular component organization or biogenesis | 2 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005488 | binding | 1 | 6 |
GO:0043167 | ion binding | 2 | 6 |
GO:0043169 | cation binding | 3 | 6 |
GO:0046872 | metal ion binding | 4 | 6 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 427 | 431 | PF00656 | 0.625 |
CLV_NRD_NRD_1 | 114 | 116 | PF00675 | 0.748 |
CLV_NRD_NRD_1 | 154 | 156 | PF00675 | 0.534 |
CLV_NRD_NRD_1 | 187 | 189 | PF00675 | 0.588 |
CLV_NRD_NRD_1 | 190 | 192 | PF00675 | 0.538 |
CLV_NRD_NRD_1 | 220 | 222 | PF00675 | 0.539 |
CLV_NRD_NRD_1 | 230 | 232 | PF00675 | 0.613 |
CLV_NRD_NRD_1 | 276 | 278 | PF00675 | 0.751 |
CLV_NRD_NRD_1 | 37 | 39 | PF00675 | 0.589 |
CLV_NRD_NRD_1 | 583 | 585 | PF00675 | 0.714 |
CLV_NRD_NRD_1 | 588 | 590 | PF00675 | 0.689 |
CLV_PCSK_FUR_1 | 188 | 192 | PF00082 | 0.662 |
CLV_PCSK_FUR_1 | 274 | 278 | PF00082 | 0.775 |
CLV_PCSK_KEX2_1 | 189 | 191 | PF00082 | 0.599 |
CLV_PCSK_KEX2_1 | 219 | 221 | PF00082 | 0.514 |
CLV_PCSK_KEX2_1 | 232 | 234 | PF00082 | 0.624 |
CLV_PCSK_KEX2_1 | 276 | 278 | PF00082 | 0.751 |
CLV_PCSK_KEX2_1 | 37 | 39 | PF00082 | 0.589 |
CLV_PCSK_KEX2_1 | 583 | 585 | PF00082 | 0.714 |
CLV_PCSK_KEX2_1 | 588 | 590 | PF00082 | 0.689 |
CLV_PCSK_PC1ET2_1 | 189 | 191 | PF00082 | 0.668 |
CLV_PCSK_PC1ET2_1 | 232 | 234 | PF00082 | 0.642 |
CLV_PCSK_PC7_1 | 584 | 590 | PF00082 | 0.699 |
CLV_PCSK_SKI1_1 | 449 | 453 | PF00082 | 0.668 |
CLV_PCSK_SKI1_1 | 564 | 568 | PF00082 | 0.700 |
CLV_PCSK_SKI1_1 | 622 | 626 | PF00082 | 0.625 |
DOC_CYCLIN_RxL_1 | 69 | 80 | PF00134 | 0.752 |
DOC_CYCLIN_yCln2_LP_2 | 55 | 61 | PF00134 | 0.704 |
DOC_CYCLIN_yCln2_LP_2 | 552 | 558 | PF00134 | 0.630 |
DOC_MAPK_gen_1 | 158 | 168 | PF00069 | 0.659 |
DOC_MAPK_gen_1 | 231 | 242 | PF00069 | 0.699 |
DOC_MAPK_MEF2A_6 | 20 | 29 | PF00069 | 0.592 |
DOC_PP1_RVXF_1 | 433 | 440 | PF00149 | 0.615 |
DOC_PP2B_LxvP_1 | 74 | 77 | PF13499 | 0.757 |
DOC_PP4_FxxP_1 | 305 | 308 | PF00568 | 0.719 |
DOC_SPAK_OSR1_1 | 617 | 621 | PF12202 | 0.661 |
DOC_USP7_MATH_1 | 106 | 110 | PF00917 | 0.714 |
DOC_USP7_MATH_1 | 247 | 251 | PF00917 | 0.717 |
DOC_USP7_MATH_1 | 255 | 259 | PF00917 | 0.775 |
DOC_USP7_MATH_1 | 261 | 265 | PF00917 | 0.835 |
DOC_USP7_MATH_1 | 290 | 294 | PF00917 | 0.663 |
DOC_USP7_MATH_1 | 309 | 313 | PF00917 | 0.555 |
DOC_USP7_MATH_1 | 331 | 335 | PF00917 | 0.708 |
DOC_USP7_MATH_1 | 354 | 358 | PF00917 | 0.798 |
DOC_USP7_MATH_1 | 361 | 365 | PF00917 | 0.718 |
DOC_USP7_MATH_1 | 484 | 488 | PF00917 | 0.844 |
DOC_USP7_MATH_1 | 505 | 509 | PF00917 | 0.660 |
DOC_USP7_MATH_1 | 75 | 79 | PF00917 | 0.661 |
DOC_USP7_MATH_2 | 518 | 524 | PF00917 | 0.734 |
DOC_WW_Pin1_4 | 249 | 254 | PF00397 | 0.710 |
DOC_WW_Pin1_4 | 327 | 332 | PF00397 | 0.757 |
DOC_WW_Pin1_4 | 355 | 360 | PF00397 | 0.720 |
DOC_WW_Pin1_4 | 384 | 389 | PF00397 | 0.627 |
DOC_WW_Pin1_4 | 524 | 529 | PF00397 | 0.740 |
DOC_WW_Pin1_4 | 532 | 537 | PF00397 | 0.753 |
DOC_WW_Pin1_4 | 54 | 59 | PF00397 | 0.710 |
DOC_WW_Pin1_4 | 8 | 13 | PF00397 | 0.563 |
LIG_14-3-3_CanoR_1 | 104 | 112 | PF00244 | 0.671 |
LIG_14-3-3_CanoR_1 | 151 | 159 | PF00244 | 0.551 |
LIG_14-3-3_CanoR_1 | 233 | 242 | PF00244 | 0.633 |
LIG_14-3-3_CanoR_1 | 274 | 283 | PF00244 | 0.755 |
LIG_14-3-3_CanoR_1 | 599 | 606 | PF00244 | 0.617 |
LIG_14-3-3_CanoR_1 | 79 | 85 | PF00244 | 0.786 |
LIG_BIR_III_4 | 297 | 301 | PF00653 | 0.723 |
LIG_BIR_III_4 | 342 | 346 | PF00653 | 0.757 |
LIG_FHA_1 | 339 | 345 | PF00498 | 0.781 |
LIG_FHA_1 | 373 | 379 | PF00498 | 0.717 |
LIG_FHA_1 | 501 | 507 | PF00498 | 0.721 |
LIG_FHA_2 | 29 | 35 | PF00498 | 0.735 |
LIG_FHA_2 | 40 | 46 | PF00498 | 0.512 |
LIG_FHA_2 | 425 | 431 | PF00498 | 0.577 |
LIG_FHA_2 | 593 | 599 | PF00498 | 0.633 |
LIG_LIR_Gen_1 | 141 | 152 | PF02991 | 0.530 |
LIG_LIR_Gen_1 | 45 | 54 | PF02991 | 0.615 |
LIG_LIR_Gen_1 | 595 | 604 | PF02991 | 0.626 |
LIG_LIR_Nem_3 | 141 | 147 | PF02991 | 0.620 |
LIG_LIR_Nem_3 | 45 | 49 | PF02991 | 0.600 |
LIG_LIR_Nem_3 | 595 | 600 | PF02991 | 0.635 |
LIG_Pex14_1 | 36 | 40 | PF04695 | 0.619 |
LIG_REV1ctd_RIR_1 | 616 | 626 | PF16727 | 0.578 |
LIG_SH2_CRK | 144 | 148 | PF00017 | 0.636 |
LIG_SH2_CRK | 40 | 44 | PF00017 | 0.700 |
LIG_SH2_CRK | 578 | 582 | PF00017 | 0.585 |
LIG_SH2_SRC | 314 | 317 | PF00017 | 0.758 |
LIG_SH2_STAP1 | 135 | 139 | PF00017 | 0.522 |
LIG_SH2_STAP1 | 22 | 26 | PF00017 | 0.770 |
LIG_SH2_STAP1 | 433 | 437 | PF00017 | 0.753 |
LIG_SH2_STAT3 | 184 | 187 | PF00017 | 0.580 |
LIG_SH2_STAT5 | 121 | 124 | PF00017 | 0.632 |
LIG_SH2_STAT5 | 144 | 147 | PF00017 | 0.472 |
LIG_SH2_STAT5 | 184 | 187 | PF00017 | 0.580 |
LIG_SH2_STAT5 | 409 | 412 | PF00017 | 0.367 |
LIG_SH3_1 | 376 | 382 | PF00018 | 0.672 |
LIG_SH3_1 | 588 | 594 | PF00018 | 0.665 |
LIG_SH3_3 | 170 | 176 | PF00018 | 0.605 |
LIG_SH3_3 | 210 | 216 | PF00018 | 0.552 |
LIG_SH3_3 | 280 | 286 | PF00018 | 0.777 |
LIG_SH3_3 | 376 | 382 | PF00018 | 0.765 |
LIG_SH3_3 | 499 | 505 | PF00018 | 0.819 |
LIG_SH3_3 | 512 | 518 | PF00018 | 0.650 |
LIG_SH3_3 | 547 | 553 | PF00018 | 0.726 |
LIG_SH3_3 | 587 | 593 | PF00018 | 0.675 |
LIG_SUMO_SIM_anti_2 | 163 | 170 | PF11976 | 0.457 |
LIG_TRAF2_1 | 130 | 133 | PF00917 | 0.650 |
LIG_TRAF2_1 | 313 | 316 | PF00917 | 0.793 |
LIG_TRAF2_1 | 474 | 477 | PF00917 | 0.743 |
LIG_TRAF2_1 | 517 | 520 | PF00917 | 0.767 |
LIG_WW_2 | 550 | 553 | PF00397 | 0.618 |
LIG_WW_3 | 1 | 5 | PF00397 | 0.761 |
MOD_CDK_SPK_2 | 384 | 389 | PF00069 | 0.627 |
MOD_CDK_SPxxK_3 | 384 | 391 | PF00069 | 0.619 |
MOD_CK1_1 | 254 | 260 | PF00069 | 0.735 |
MOD_CK1_1 | 263 | 269 | PF00069 | 0.741 |
MOD_CK1_1 | 293 | 299 | PF00069 | 0.785 |
MOD_CK1_1 | 310 | 316 | PF00069 | 0.685 |
MOD_CK1_1 | 317 | 323 | PF00069 | 0.719 |
MOD_CK1_1 | 327 | 333 | PF00069 | 0.645 |
MOD_CK1_1 | 357 | 363 | PF00069 | 0.725 |
MOD_CK1_1 | 465 | 471 | PF00069 | 0.580 |
MOD_CK1_1 | 78 | 84 | PF00069 | 0.815 |
MOD_CK2_1 | 266 | 272 | PF00069 | 0.850 |
MOD_CK2_1 | 28 | 34 | PF00069 | 0.740 |
MOD_CK2_1 | 293 | 299 | PF00069 | 0.730 |
MOD_CK2_1 | 310 | 316 | PF00069 | 0.739 |
MOD_CK2_1 | 39 | 45 | PF00069 | 0.702 |
MOD_CK2_1 | 442 | 448 | PF00069 | 0.809 |
MOD_CK2_1 | 484 | 490 | PF00069 | 0.719 |
MOD_CK2_1 | 592 | 598 | PF00069 | 0.636 |
MOD_CK2_1 | 8 | 14 | PF00069 | 0.776 |
MOD_GlcNHglycan | 108 | 111 | PF01048 | 0.682 |
MOD_GlcNHglycan | 253 | 256 | PF01048 | 0.725 |
MOD_GlcNHglycan | 257 | 260 | PF01048 | 0.747 |
MOD_GlcNHglycan | 363 | 366 | PF01048 | 0.801 |
MOD_GlcNHglycan | 444 | 447 | PF01048 | 0.776 |
MOD_GlcNHglycan | 466 | 470 | PF01048 | 0.696 |
MOD_GlcNHglycan | 486 | 489 | PF01048 | 0.815 |
MOD_GlcNHglycan | 520 | 525 | PF01048 | 0.864 |
MOD_GlcNHglycan | 64 | 68 | PF01048 | 0.604 |
MOD_GlcNHglycan | 81 | 84 | PF01048 | 0.735 |
MOD_GSK3_1 | 247 | 254 | PF00069 | 0.671 |
MOD_GSK3_1 | 255 | 262 | PF00069 | 0.723 |
MOD_GSK3_1 | 263 | 270 | PF00069 | 0.736 |
MOD_GSK3_1 | 310 | 317 | PF00069 | 0.727 |
MOD_GSK3_1 | 327 | 334 | PF00069 | 0.735 |
MOD_GSK3_1 | 357 | 364 | PF00069 | 0.725 |
MOD_GSK3_1 | 420 | 427 | PF00069 | 0.440 |
MOD_GSK3_1 | 478 | 485 | PF00069 | 0.717 |
MOD_GSK3_1 | 520 | 527 | PF00069 | 0.670 |
MOD_GSK3_1 | 75 | 82 | PF00069 | 0.707 |
MOD_N-GLC_1 | 327 | 332 | PF02516 | 0.725 |
MOD_N-GLC_1 | 382 | 387 | PF02516 | 0.644 |
MOD_N-GLC_1 | 462 | 467 | PF02516 | 0.677 |
MOD_N-GLC_1 | 524 | 529 | PF02516 | 0.667 |
MOD_NEK2_1 | 143 | 148 | PF00069 | 0.556 |
MOD_NEK2_2 | 150 | 155 | PF00069 | 0.521 |
MOD_NEK2_2 | 39 | 44 | PF00069 | 0.703 |
MOD_PIKK_1 | 128 | 134 | PF00454 | 0.567 |
MOD_PIKK_1 | 191 | 197 | PF00454 | 0.572 |
MOD_PIKK_1 | 284 | 290 | PF00454 | 0.630 |
MOD_PKA_1 | 276 | 282 | PF00069 | 0.697 |
MOD_PKA_2 | 150 | 156 | PF00069 | 0.543 |
MOD_PKA_2 | 264 | 270 | PF00069 | 0.761 |
MOD_PKA_2 | 275 | 281 | PF00069 | 0.716 |
MOD_PKA_2 | 598 | 604 | PF00069 | 0.620 |
MOD_PKA_2 | 78 | 84 | PF00069 | 0.702 |
MOD_PKB_1 | 231 | 239 | PF00069 | 0.752 |
MOD_PKB_1 | 274 | 282 | PF00069 | 0.681 |
MOD_Plk_1 | 236 | 242 | PF00069 | 0.649 |
MOD_Plk_1 | 429 | 435 | PF00069 | 0.740 |
MOD_Plk_1 | 564 | 570 | PF00069 | 0.691 |
MOD_Plk_2-3 | 543 | 549 | PF00069 | 0.730 |
MOD_Plk_2-3 | 598 | 604 | PF00069 | 0.620 |
MOD_Plk_4 | 236 | 242 | PF00069 | 0.649 |
MOD_Plk_4 | 592 | 598 | PF00069 | 0.636 |
MOD_ProDKin_1 | 249 | 255 | PF00069 | 0.712 |
MOD_ProDKin_1 | 327 | 333 | PF00069 | 0.756 |
MOD_ProDKin_1 | 355 | 361 | PF00069 | 0.714 |
MOD_ProDKin_1 | 384 | 390 | PF00069 | 0.620 |
MOD_ProDKin_1 | 524 | 530 | PF00069 | 0.741 |
MOD_ProDKin_1 | 532 | 538 | PF00069 | 0.752 |
MOD_ProDKin_1 | 54 | 60 | PF00069 | 0.715 |
MOD_ProDKin_1 | 8 | 14 | PF00069 | 0.560 |
MOD_SUMO_for_1 | 200 | 203 | PF00179 | 0.633 |
TRG_DiLeu_BaEn_1 | 164 | 169 | PF01217 | 0.672 |
TRG_DiLeu_BaEn_1 | 608 | 613 | PF01217 | 0.570 |
TRG_DiLeu_BaLyEn_6 | 50 | 55 | PF01217 | 0.733 |
TRG_ENDOCYTIC_2 | 144 | 147 | PF00928 | 0.528 |
TRG_ENDOCYTIC_2 | 22 | 25 | PF00928 | 0.774 |
TRG_ENDOCYTIC_2 | 40 | 43 | PF00928 | 0.690 |
TRG_ENDOCYTIC_2 | 578 | 581 | PF00928 | 0.740 |
TRG_ENDOCYTIC_2 | 597 | 600 | PF00928 | 0.627 |
TRG_ER_diArg_1 | 188 | 191 | PF00400 | 0.664 |
TRG_ER_diArg_1 | 219 | 221 | PF00400 | 0.550 |
TRG_ER_diArg_1 | 230 | 233 | PF00400 | 0.626 |
TRG_ER_diArg_1 | 274 | 277 | PF00400 | 0.836 |
TRG_ER_diArg_1 | 3 | 6 | PF00400 | 0.759 |
TRG_ER_diArg_1 | 36 | 38 | PF00400 | 0.623 |
TRG_ER_diArg_1 | 388 | 391 | PF00400 | 0.586 |
TRG_ER_diArg_1 | 588 | 590 | PF00400 | 0.693 |
TRG_NLS_Bipartite_1 | 219 | 236 | PF00514 | 0.591 |
TRG_NLS_MonoCore_2 | 187 | 192 | PF00514 | 0.659 |
TRG_NLS_MonoCore_2 | 231 | 236 | PF00514 | 0.751 |
TRG_NLS_MonoExtC_3 | 154 | 159 | PF00514 | 0.648 |
TRG_NLS_MonoExtC_3 | 188 | 193 | PF00514 | 0.662 |
TRG_NLS_MonoExtC_3 | 230 | 235 | PF00514 | 0.643 |
TRG_NLS_MonoExtN_4 | 188 | 193 | PF00514 | 0.662 |
TRG_NLS_MonoExtN_4 | 231 | 236 | PF00514 | 0.751 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I7Y7 | Leptomonas seymouri | 48% | 100% |
A4I4B3 | Leishmania infantum | 99% | 100% |
E9ADR3 | Leishmania major | 85% | 100% |
E9AIT5 | Leishmania braziliensis | 69% | 99% |
E9AM17 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 86% | 100% |