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 |
Related structures:
AlphaFold database: A4HID8
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 12 | 14 | PF00675 | 0.568 |
CLV_NRD_NRD_1 | 125 | 127 | PF00675 | 0.685 |
CLV_NRD_NRD_1 | 154 | 156 | PF00675 | 0.703 |
CLV_NRD_NRD_1 | 206 | 208 | PF00675 | 0.589 |
CLV_NRD_NRD_1 | 289 | 291 | PF00675 | 0.638 |
CLV_NRD_NRD_1 | 303 | 305 | PF00675 | 0.554 |
CLV_NRD_NRD_1 | 70 | 72 | PF00675 | 0.623 |
CLV_NRD_NRD_1 | 95 | 97 | PF00675 | 0.622 |
CLV_PCSK_FUR_1 | 123 | 127 | PF00082 | 0.703 |
CLV_PCSK_FUR_1 | 68 | 72 | PF00082 | 0.720 |
CLV_PCSK_KEX2_1 | 12 | 14 | PF00082 | 0.557 |
CLV_PCSK_KEX2_1 | 125 | 127 | PF00082 | 0.696 |
CLV_PCSK_KEX2_1 | 154 | 156 | PF00082 | 0.703 |
CLV_PCSK_KEX2_1 | 289 | 291 | PF00082 | 0.637 |
CLV_PCSK_KEX2_1 | 303 | 305 | PF00082 | 0.578 |
CLV_PCSK_KEX2_1 | 70 | 72 | PF00082 | 0.624 |
CLV_PCSK_KEX2_1 | 95 | 97 | PF00082 | 0.621 |
CLV_PCSK_SKI1_1 | 96 | 100 | PF00082 | 0.652 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.632 |
DEG_SCF_FBW7_1 | 111 | 116 | PF00400 | 0.711 |
DOC_CKS1_1 | 119 | 124 | PF01111 | 0.634 |
DOC_CKS1_1 | 88 | 93 | PF01111 | 0.635 |
DOC_MAPK_DCC_7 | 196 | 204 | PF00069 | 0.629 |
DOC_MAPK_MEF2A_6 | 196 | 204 | PF00069 | 0.629 |
DOC_MAPK_MEF2A_6 | 244 | 253 | PF00069 | 0.629 |
DOC_PP2B_PxIxI_1 | 273 | 279 | PF00149 | 0.485 |
DOC_PP4_MxPP_1 | 231 | 234 | PF00568 | 0.518 |
DOC_USP7_MATH_1 | 100 | 104 | PF00917 | 0.760 |
DOC_USP7_MATH_1 | 113 | 117 | PF00917 | 0.672 |
DOC_USP7_MATH_1 | 131 | 135 | PF00917 | 0.508 |
DOC_USP7_MATH_1 | 15 | 19 | PF00917 | 0.556 |
DOC_USP7_MATH_1 | 160 | 164 | PF00917 | 0.672 |
DOC_USP7_MATH_1 | 30 | 34 | PF00917 | 0.682 |
DOC_USP7_UBL2_3 | 192 | 196 | PF12436 | 0.630 |
DOC_USP7_UBL2_3 | 205 | 209 | PF12436 | 0.456 |
DOC_WW_Pin1_4 | 109 | 114 | PF00397 | 0.694 |
DOC_WW_Pin1_4 | 118 | 123 | PF00397 | 0.628 |
DOC_WW_Pin1_4 | 132 | 137 | PF00397 | 0.563 |
DOC_WW_Pin1_4 | 255 | 260 | PF00397 | 0.648 |
DOC_WW_Pin1_4 | 278 | 283 | PF00397 | 0.657 |
DOC_WW_Pin1_4 | 297 | 302 | PF00397 | 0.582 |
DOC_WW_Pin1_4 | 62 | 67 | PF00397 | 0.740 |
DOC_WW_Pin1_4 | 87 | 92 | PF00397 | 0.604 |
DOC_WW_Pin1_4 | 96 | 101 | PF00397 | 0.645 |
LIG_14-3-3_CanoR_1 | 114 | 122 | PF00244 | 0.674 |
LIG_14-3-3_CanoR_1 | 162 | 167 | PF00244 | 0.663 |
LIG_14-3-3_CanoR_1 | 173 | 181 | PF00244 | 0.544 |
LIG_14-3-3_CanoR_1 | 218 | 225 | PF00244 | 0.484 |
LIG_14-3-3_CanoR_1 | 303 | 307 | PF00244 | 0.567 |
LIG_14-3-3_CanoR_1 | 48 | 55 | PF00244 | 0.457 |
LIG_APCC_ABBA_1 | 211 | 216 | PF00400 | 0.486 |
LIG_deltaCOP1_diTrp_1 | 243 | 248 | PF00928 | 0.614 |
LIG_eIF4E_2 | 127 | 133 | PF01652 | 0.471 |
LIG_FHA_1 | 303 | 309 | PF00498 | 0.585 |
LIG_FHA_2 | 2 | 8 | PF00498 | 0.671 |
LIG_LIR_Gen_1 | 18 | 24 | PF02991 | 0.645 |
LIG_LIR_Gen_1 | 243 | 253 | PF02991 | 0.626 |
LIG_LIR_Gen_1 | 305 | 314 | PF02991 | 0.497 |
LIG_LIR_Nem_3 | 18 | 23 | PF02991 | 0.643 |
LIG_LIR_Nem_3 | 243 | 249 | PF02991 | 0.616 |
LIG_LIR_Nem_3 | 305 | 309 | PF02991 | 0.507 |
LIG_MYND_1 | 199 | 203 | PF01753 | 0.544 |
LIG_MYND_1 | 283 | 287 | PF01753 | 0.483 |
LIG_SH2_PTP2 | 127 | 130 | PF00017 | 0.659 |
LIG_SH2_SRC | 127 | 130 | PF00017 | 0.645 |
LIG_SH2_STAP1 | 55 | 59 | PF00017 | 0.664 |
LIG_SH2_STAT5 | 127 | 130 | PF00017 | 0.670 |
LIG_SH3_1 | 133 | 139 | PF00018 | 0.535 |
LIG_SH3_1 | 230 | 236 | PF00018 | 0.520 |
LIG_SH3_2 | 200 | 205 | PF14604 | 0.631 |
LIG_SH3_2 | 284 | 289 | PF14604 | 0.488 |
LIG_SH3_3 | 116 | 122 | PF00018 | 0.705 |
LIG_SH3_3 | 125 | 131 | PF00018 | 0.690 |
LIG_SH3_3 | 133 | 139 | PF00018 | 0.550 |
LIG_SH3_3 | 184 | 190 | PF00018 | 0.666 |
LIG_SH3_3 | 194 | 200 | PF00018 | 0.555 |
LIG_SH3_3 | 229 | 235 | PF00018 | 0.469 |
LIG_SH3_3 | 268 | 274 | PF00018 | 0.687 |
LIG_SH3_3 | 281 | 287 | PF00018 | 0.498 |
LIG_SH3_3 | 85 | 91 | PF00018 | 0.566 |
LIG_SH3_4 | 192 | 199 | PF00018 | 0.630 |
LIG_SH3_4 | 205 | 212 | PF00018 | 0.459 |
LIG_SUMO_SIM_par_1 | 274 | 279 | PF11976 | 0.674 |
MOD_CDC14_SPxK_1 | 135 | 138 | PF00782 | 0.522 |
MOD_CDK_SPK_2 | 109 | 114 | PF00069 | 0.691 |
MOD_CDK_SPK_2 | 118 | 123 | PF00069 | 0.705 |
MOD_CDK_SPK_2 | 87 | 92 | PF00069 | 0.650 |
MOD_CDK_SPxK_1 | 132 | 138 | PF00069 | 0.534 |
MOD_CDK_SPxK_1 | 297 | 303 | PF00069 | 0.588 |
MOD_CDK_SPxK_1 | 62 | 68 | PF00069 | 0.746 |
MOD_CDK_SPxxK_3 | 118 | 125 | PF00069 | 0.635 |
MOD_CDK_SPxxK_3 | 297 | 304 | PF00069 | 0.541 |
MOD_CK1_1 | 109 | 115 | PF00069 | 0.653 |
MOD_CK1_1 | 172 | 178 | PF00069 | 0.584 |
MOD_CK1_1 | 255 | 261 | PF00069 | 0.583 |
MOD_CK1_1 | 28 | 34 | PF00069 | 0.676 |
MOD_CK2_1 | 1 | 7 | PF00069 | 0.680 |
MOD_Cter_Amidation | 68 | 71 | PF01082 | 0.618 |
MOD_GlcNHglycan | 220 | 223 | PF01048 | 0.568 |
MOD_GlcNHglycan | 239 | 242 | PF01048 | 0.568 |
MOD_GSK3_1 | 109 | 116 | PF00069 | 0.613 |
MOD_GSK3_1 | 145 | 152 | PF00069 | 0.632 |
MOD_GSK3_1 | 154 | 161 | PF00069 | 0.714 |
MOD_GSK3_1 | 169 | 176 | PF00069 | 0.632 |
MOD_GSK3_1 | 274 | 281 | PF00069 | 0.573 |
MOD_GSK3_1 | 43 | 50 | PF00069 | 0.549 |
MOD_GSK3_1 | 96 | 103 | PF00069 | 0.646 |
MOD_N-GLC_1 | 109 | 114 | PF02516 | 0.675 |
MOD_N-GLC_1 | 149 | 154 | PF02516 | 0.664 |
MOD_N-GLC_1 | 264 | 269 | PF02516 | 0.551 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.650 |
MOD_NEK2_1 | 171 | 176 | PF00069 | 0.510 |
MOD_NEK2_1 | 47 | 52 | PF00069 | 0.461 |
MOD_NEK2_2 | 15 | 20 | PF00069 | 0.559 |
MOD_PIKK_1 | 47 | 53 | PF00454 | 0.454 |
MOD_PK_1 | 162 | 168 | PF00069 | 0.715 |
MOD_PKA_1 | 154 | 160 | PF00069 | 0.610 |
MOD_PKA_2 | 113 | 119 | PF00069 | 0.646 |
MOD_PKA_2 | 154 | 160 | PF00069 | 0.662 |
MOD_PKA_2 | 172 | 178 | PF00069 | 0.672 |
MOD_PKA_2 | 25 | 31 | PF00069 | 0.578 |
MOD_PKA_2 | 302 | 308 | PF00069 | 0.576 |
MOD_PKA_2 | 47 | 53 | PF00069 | 0.468 |
MOD_Plk_1 | 145 | 151 | PF00069 | 0.590 |
MOD_Plk_1 | 264 | 270 | PF00069 | 0.596 |
MOD_Plk_4 | 15 | 21 | PF00069 | 0.537 |
MOD_Plk_4 | 182 | 188 | PF00069 | 0.679 |
MOD_Plk_4 | 50 | 56 | PF00069 | 0.669 |
MOD_ProDKin_1 | 109 | 115 | PF00069 | 0.693 |
MOD_ProDKin_1 | 118 | 124 | PF00069 | 0.628 |
MOD_ProDKin_1 | 132 | 138 | PF00069 | 0.560 |
MOD_ProDKin_1 | 255 | 261 | PF00069 | 0.648 |
MOD_ProDKin_1 | 278 | 284 | PF00069 | 0.656 |
MOD_ProDKin_1 | 297 | 303 | PF00069 | 0.579 |
MOD_ProDKin_1 | 62 | 68 | PF00069 | 0.746 |
MOD_ProDKin_1 | 87 | 93 | PF00069 | 0.603 |
MOD_ProDKin_1 | 96 | 102 | PF00069 | 0.642 |
TRG_DiLeu_BaLyEn_6 | 197 | 202 | PF01217 | 0.539 |
TRG_ER_diArg_1 | 122 | 125 | PF00400 | 0.697 |
TRG_ER_diArg_1 | 289 | 291 | PF00400 | 0.628 |
TRG_ER_diArg_1 | 302 | 304 | PF00400 | 0.685 |
TRG_ER_diArg_1 | 67 | 70 | PF00400 | 0.750 |
TRG_ER_diArg_1 | 94 | 96 | PF00400 | 0.679 |
TRG_NLS_MonoExtN_4 | 205 | 211 | PF00514 | 0.443 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P913 | Leptomonas seymouri | 61% | 100% |
A0A1X0P1U3 | Trypanosomatidae | 29% | 100% |
A0A3Q8IFW1 | Leishmania donovani | 77% | 100% |
A0A422P3E4 | Trypanosoma rangeli | 33% | 100% |
A4I5N5 | Leishmania infantum | 77% | 100% |
E9B0X9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 75% | 100% |
Q4Q787 | Leishmania major | 76% | 99% |
V5BYT6 | Trypanosoma cruzi | 31% | 100% |