| 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:0005929 | cilium | 4 | 7 | 
| GO:0042995 | cell projection | 2 | 7 | 
| GO:0043226 | organelle | 2 | 7 | 
| GO:0043227 | membrane-bounded organelle | 3 | 7 | 
| GO:0110165 | cellular anatomical entity | 1 | 7 | 
| GO:0120025 | plasma membrane bounded cell projection | 3 | 7 | 
Related structures:
AlphaFold database: A4IA75
| Leishmania | From | To | Domain/Motif | Score | 
|---|---|---|---|---|
| CLV_C14_Caspase3-7 | 17 | 21 | PF00656 | 0.541 | 
| CLV_MEL_PAP_1 | 235 | 241 | PF00089 | 0.542 | 
| CLV_NRD_NRD_1 | 106 | 108 | PF00675 | 0.593 | 
| CLV_NRD_NRD_1 | 113 | 115 | PF00675 | 0.574 | 
| CLV_NRD_NRD_1 | 218 | 220 | PF00675 | 0.577 | 
| CLV_NRD_NRD_1 | 279 | 281 | PF00675 | 0.579 | 
| CLV_NRD_NRD_1 | 31 | 33 | PF00675 | 0.789 | 
| CLV_NRD_NRD_1 | 360 | 362 | PF00675 | 0.588 | 
| CLV_NRD_NRD_1 | 414 | 416 | PF00675 | 0.517 | 
| CLV_PCSK_FUR_1 | 111 | 115 | PF00082 | 0.656 | 
| CLV_PCSK_KEX2_1 | 106 | 108 | PF00082 | 0.691 | 
| CLV_PCSK_KEX2_1 | 113 | 115 | PF00082 | 0.554 | 
| CLV_PCSK_KEX2_1 | 218 | 220 | PF00082 | 0.580 | 
| CLV_PCSK_KEX2_1 | 279 | 281 | PF00082 | 0.556 | 
| CLV_PCSK_KEX2_1 | 31 | 33 | PF00082 | 0.732 | 
| CLV_PCSK_KEX2_1 | 360 | 362 | PF00082 | 0.490 | 
| CLV_PCSK_PC7_1 | 356 | 362 | PF00082 | 0.500 | 
| CLV_PCSK_SKI1_1 | 371 | 375 | PF00082 | 0.578 | 
| DEG_APCC_DBOX_1 | 355 | 363 | PF00400 | 0.494 | 
| DEG_SCF_FBW7_1 | 150 | 156 | PF00400 | 0.612 | 
| DOC_CKS1_1 | 150 | 155 | PF01111 | 0.708 | 
| DOC_MAPK_gen_1 | 106 | 112 | PF00069 | 0.546 | 
| DOC_MAPK_gen_1 | 218 | 229 | PF00069 | 0.502 | 
| DOC_MAPK_gen_1 | 279 | 285 | PF00069 | 0.568 | 
| DOC_MAPK_gen_1 | 360 | 367 | PF00069 | 0.563 | 
| DOC_MAPK_MEF2A_6 | 330 | 338 | PF00069 | 0.573 | 
| DOC_PIKK_1 | 68 | 76 | PF02985 | 0.716 | 
| DOC_USP7_MATH_1 | 169 | 173 | PF00917 | 0.722 | 
| DOC_WW_Pin1_4 | 123 | 128 | PF00397 | 0.684 | 
| DOC_WW_Pin1_4 | 140 | 145 | PF00397 | 0.563 | 
| DOC_WW_Pin1_4 | 149 | 154 | PF00397 | 0.673 | 
| DOC_WW_Pin1_4 | 261 | 266 | PF00397 | 0.690 | 
| DOC_WW_Pin1_4 | 268 | 273 | PF00397 | 0.690 | 
| DOC_WW_Pin1_4 | 37 | 42 | PF00397 | 0.674 | 
| DOC_WW_Pin1_4 | 385 | 390 | PF00397 | 0.585 | 
| LIG_14-3-3_CanoR_1 | 106 | 112 | PF00244 | 0.541 | 
| LIG_14-3-3_CanoR_1 | 121 | 129 | PF00244 | 0.602 | 
| LIG_14-3-3_CanoR_1 | 137 | 145 | PF00244 | 0.522 | 
| LIG_14-3-3_CanoR_1 | 15 | 22 | PF00244 | 0.581 | 
| LIG_14-3-3_CanoR_1 | 279 | 283 | PF00244 | 0.645 | 
| LIG_14-3-3_CanoR_1 | 330 | 334 | PF00244 | 0.511 | 
| LIG_14-3-3_CanoR_1 | 397 | 402 | PF00244 | 0.573 | 
| LIG_14-3-3_CanoR_1 | 403 | 407 | PF00244 | 0.487 | 
| LIG_Actin_WH2_2 | 282 | 298 | PF00022 | 0.641 | 
| LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.658 | 
| LIG_DLG_GKlike_1 | 397 | 405 | PF00625 | 0.506 | 
| LIG_FHA_1 | 145 | 151 | PF00498 | 0.734 | 
| LIG_FHA_1 | 197 | 203 | PF00498 | 0.634 | 
| LIG_FHA_1 | 286 | 292 | PF00498 | 0.593 | 
| LIG_FHA_1 | 372 | 378 | PF00498 | 0.466 | 
| LIG_FHA_2 | 126 | 132 | PF00498 | 0.770 | 
| LIG_FHA_2 | 137 | 143 | PF00498 | 0.697 | 
| LIG_FHA_2 | 179 | 185 | PF00498 | 0.739 | 
| LIG_FHA_2 | 64 | 70 | PF00498 | 0.689 | 
| LIG_FHA_2 | 79 | 85 | PF00498 | 0.542 | 
| LIG_LIR_Gen_1 | 10 | 16 | PF02991 | 0.653 | 
| LIG_LIR_Gen_1 | 281 | 290 | PF02991 | 0.622 | 
| LIG_LIR_Nem_3 | 10 | 14 | PF02991 | 0.654 | 
| LIG_LIR_Nem_3 | 281 | 285 | PF02991 | 0.635 | 
| LIG_MYND_1 | 261 | 265 | PF01753 | 0.572 | 
| LIG_SH2_STAP1 | 145 | 149 | PF00017 | 0.603 | 
| LIG_SH2_STAP1 | 300 | 304 | PF00017 | 0.495 | 
| LIG_SH2_STAT3 | 200 | 203 | PF00017 | 0.625 | 
| LIG_SH2_STAT5 | 200 | 203 | PF00017 | 0.578 | 
| LIG_SH2_STAT5 | 220 | 223 | PF00017 | 0.338 | 
| LIG_SH2_STAT5 | 358 | 361 | PF00017 | 0.591 | 
| LIG_SH3_3 | 259 | 265 | PF00018 | 0.747 | 
| LIG_SUMO_SIM_par_1 | 288 | 294 | PF11976 | 0.603 | 
| LIG_SUMO_SIM_par_1 | 363 | 368 | PF11976 | 0.550 | 
| LIG_SUMO_SIM_par_1 | 46 | 53 | PF11976 | 0.651 | 
| LIG_TRAF2_1 | 189 | 192 | PF00917 | 0.693 | 
| LIG_TRAF2_1 | 81 | 84 | PF00917 | 0.631 | 
| LIG_WRC_WIRS_1 | 251 | 256 | PF05994 | 0.650 | 
| MOD_CDC14_SPxK_1 | 276 | 279 | PF00782 | 0.577 | 
| MOD_CDK_SPxK_1 | 149 | 155 | PF00069 | 0.609 | 
| MOD_CDK_SPxK_1 | 268 | 274 | PF00069 | 0.597 | 
| MOD_CDK_SPxxK_3 | 273 | 280 | PF00069 | 0.721 | 
| MOD_CK1_1 | 123 | 129 | PF00069 | 0.669 | 
| MOD_CK1_1 | 151 | 157 | PF00069 | 0.757 | 
| MOD_CK1_1 | 402 | 408 | PF00069 | 0.465 | 
| MOD_CK2_1 | 178 | 184 | PF00069 | 0.769 | 
| MOD_CK2_1 | 78 | 84 | PF00069 | 0.648 | 
| MOD_Cter_Amidation | 277 | 280 | PF01082 | 0.567 | 
| MOD_GlcNHglycan | 157 | 160 | PF01048 | 0.706 | 
| MOD_GlcNHglycan | 164 | 167 | PF01048 | 0.679 | 
| MOD_GlcNHglycan | 170 | 174 | PF01048 | 0.657 | 
| MOD_GlcNHglycan | 231 | 234 | PF01048 | 0.523 | 
| MOD_GlcNHglycan | 305 | 309 | PF01048 | 0.501 | 
| MOD_GlcNHglycan | 366 | 370 | PF01048 | 0.550 | 
| MOD_GSK3_1 | 136 | 143 | PF00069 | 0.692 | 
| MOD_GSK3_1 | 144 | 151 | PF00069 | 0.681 | 
| MOD_GSK3_1 | 243 | 250 | PF00069 | 0.643 | 
| MOD_GSK3_1 | 281 | 288 | PF00069 | 0.584 | 
| MOD_GSK3_1 | 365 | 372 | PF00069 | 0.443 | 
| MOD_GSK3_1 | 397 | 404 | PF00069 | 0.502 | 
| MOD_GSK3_1 | 60 | 67 | PF00069 | 0.719 | 
| MOD_GSK3_1 | 74 | 81 | PF00069 | 0.569 | 
| MOD_N-GLC_1 | 369 | 374 | PF02516 | 0.452 | 
| MOD_N-GLC_1 | 74 | 79 | PF02516 | 0.681 | 
| MOD_NEK2_1 | 1 | 6 | PF00069 | 0.644 | 
| MOD_NEK2_1 | 14 | 19 | PF00069 | 0.648 | 
| MOD_NEK2_1 | 247 | 252 | PF00069 | 0.639 | 
| MOD_NEK2_1 | 338 | 343 | PF00069 | 0.452 | 
| MOD_NEK2_1 | 365 | 370 | PF00069 | 0.547 | 
| MOD_NEK2_1 | 384 | 389 | PF00069 | 0.258 | 
| MOD_NEK2_1 | 401 | 406 | PF00069 | 0.294 | 
| MOD_PIKK_1 | 1 | 7 | PF00454 | 0.702 | 
| MOD_PIKK_1 | 86 | 92 | PF00454 | 0.585 | 
| MOD_PKA_2 | 105 | 111 | PF00069 | 0.547 | 
| MOD_PKA_2 | 120 | 126 | PF00069 | 0.569 | 
| MOD_PKA_2 | 136 | 142 | PF00069 | 0.542 | 
| MOD_PKA_2 | 14 | 20 | PF00069 | 0.598 | 
| MOD_PKA_2 | 154 | 160 | PF00069 | 0.547 | 
| MOD_PKA_2 | 229 | 235 | PF00069 | 0.453 | 
| MOD_PKA_2 | 237 | 243 | PF00069 | 0.526 | 
| MOD_PKA_2 | 278 | 284 | PF00069 | 0.543 | 
| MOD_PKA_2 | 329 | 335 | PF00069 | 0.509 | 
| MOD_PKA_2 | 396 | 402 | PF00069 | 0.568 | 
| MOD_Plk_1 | 369 | 375 | PF00069 | 0.454 | 
| MOD_Plk_1 | 74 | 80 | PF00069 | 0.752 | 
| MOD_Plk_1 | 9 | 15 | PF00069 | 0.599 | 
| MOD_Plk_4 | 125 | 131 | PF00069 | 0.732 | 
| MOD_Plk_4 | 196 | 202 | PF00069 | 0.675 | 
| MOD_Plk_4 | 243 | 249 | PF00069 | 0.555 | 
| MOD_Plk_4 | 285 | 291 | PF00069 | 0.539 | 
| MOD_Plk_4 | 329 | 335 | PF00069 | 0.509 | 
| MOD_ProDKin_1 | 123 | 129 | PF00069 | 0.695 | 
| MOD_ProDKin_1 | 140 | 146 | PF00069 | 0.564 | 
| MOD_ProDKin_1 | 149 | 155 | PF00069 | 0.676 | 
| MOD_ProDKin_1 | 261 | 267 | PF00069 | 0.688 | 
| MOD_ProDKin_1 | 268 | 274 | PF00069 | 0.692 | 
| MOD_ProDKin_1 | 37 | 43 | PF00069 | 0.672 | 
| MOD_ProDKin_1 | 385 | 391 | PF00069 | 0.578 | 
| TRG_DiLeu_BaEn_4 | 192 | 198 | PF01217 | 0.722 | 
| TRG_DiLeu_BaLyEn_6 | 386 | 391 | PF01217 | 0.485 | 
| TRG_ER_diArg_1 | 110 | 113 | PF00400 | 0.581 | 
| TRG_ER_diArg_1 | 218 | 220 | PF00400 | 0.570 | 
| TRG_ER_diArg_1 | 30 | 32 | PF00400 | 0.693 | 
| TRG_ER_diArg_1 | 359 | 361 | PF00400 | 0.591 | 
| Protein | Taxonomy | Sequence identity | Coverage | 
|---|---|---|---|
| A0A0N1PBH6 | Leptomonas seymouri | 44% | 100% | 
| A0A3Q8IIQ7 | Leishmania donovani | 100% | 100% | 
| A4HB18 | Leishmania braziliensis | 68% | 100% | 
| E9B588 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 87% | 100% | 
| Q4Q2P5 | Leishmania major | 90% | 100% |